Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51130 |
| ensemblid | ENSG00000115239.24 |
| hgncid | 16013 |
| symbol | ASB3 |
| name | ankyrin repeat and SOCS box containing 3 |
| refseq_nuc | NM_016115.5 |
| refseq_prot | NP_057199.1 |
| ensembl_nuc | ENST00000263634.8 |
| ensembl_prot | ENSP00000263634.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 53669980 |
| end | 53786953 |
| strand | - |
| ver | v1.2 |
| region | chr2:53669980-53786953 |
| region5000 | chr2:53664980-53791953 |
| regionname0 | ASB3_chr2_53669980_53786953 |
| regionname5000 | ASB3_chr2_53664980_53791953 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 518 | 335 | 84 | 56 | 147 | 12 | 35 | 109 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0002 | 0/0 | 518 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0003 | 0/1 | 518 | 4 | 1 | 2 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0004 | 0/0 | 518 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0005 | 0/0 | 518 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0006 | 0/0 | 518 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| a0007 | 0/0 | 518 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | MDFTE others(513): Show |
chr2 | 53664980 | 53791953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1554 | 241 | 77 | 42 | 88 | 10 | 23 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0001c0002 | 0/0 | 1554 | 49 | 1 | 0 | 39 | 2 | 7 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0001c0003 | 0/0 | 1554 | 45 | 6 | 14 | 20 | 0 | 5 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0002c0004 | 0/0 | 1554 | 5 | 5 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0003c0005 | 0/1 | 1554 | 4 | 1 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0004c0008 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0004c0009 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0005c0006 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0006c0010 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 | ||
| a0007c0007 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | ATGGA others(1549): Show |
chr2 | 53664980 | 53791953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2226 | 144 | 43 | 24 | 53 | 5 | 18 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0002 | 0/0 | 2226 | 8 | 4 | 2 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0003 | 0/0 | 2225 | 41 | 10 | 9 | 18 | 2 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0004 | 0/0 | 2227 | 26 | 13 | 4 | 7 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0005 | 0/0 | 2219 | 2 | 0 | 0 | 0 | 2 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2214): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0006 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0007 | 0/0 | 2225 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0008 | 0/0 | 2224 | 8 | 5 | 1 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2219): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0009 | 0/0 | 2225 | 5 | 0 | 1 | 4 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0011 | 0/0 | 2226 | 2 | 0 | 0 | 0 | 1 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0012 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0001t0015 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0002t0001 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0002t0002 | 0/0 | 2226 | 39 | 1 | 0 | 30 | 2 | 6 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0002t0006 | 0/0 | 2227 | 5 | 0 | 0 | 5 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0001c0002t0007 | 0/0 | 2225 | 4 | 0 | 0 | 3 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0001 | 0/0 | 2226 | 3 | 0 | 3 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0002 | 0/0 | 2226 | 25 | 5 | 3 | 16 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0003 | 0/0 | 2225 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0004 | 0/0 | 2227 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0005 | 0/0 | 2219 | 7 | 0 | 5 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2214): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0006 | 0/0 | 2227 | 3 | 0 | 1 | 1 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0007 | 0/0 | 2225 | 3 | 1 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2220): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0011 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0001c0003t0014 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0002c0004t0010 | 0/0 | 2226 | 4 | 4 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0002c0004t0013 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2222): Show |
chr2 | 53664980 | 53791953 |
| a0003c0005t0005 | 0/1 | 2219 | 4 | 1 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2214): Show |
chr2 | 53664980 | 53791953 |
| a0004c0008t0001 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0004c0009t0001 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0005c0006t0002 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0006c0010t0001 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2221): Show |
chr2 | 53664980 | 53791953 |
| a0007c0007t0005 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | GTCGC others(2214): Show |
chr2 | 53664980 | 53791953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0011g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0014g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0004c0008t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0004c0009t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0005c0006t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0005c0006t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0006c0010t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0007c0007t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0010 | t0001 | g0099 | EUR | GBR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0244 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00323 | hp1 | a0001 | c0001 | t0011 | g0095 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0220 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00558 | hp2 | a0001 | c0003 | t0007 | g0283 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0309 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00733 | hp1 | a0001 | c0003 | t0005 | g0328 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0301 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0302 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01106 | hp2 | a0003 | c0005 | t0005 | g0337 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0304 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01168 | hp1 | a0001 | c0003 | t0005 | g0311 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0305 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0290 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01192 | hp1 | a0001 | c0003 | t0005 | g0343 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0033 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01256 | hp2 | a0001 | c0003 | t0011 | g0329 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01257 | hp2 | a0001 | c0003 | t0005 | g0330 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01261 | hp2 | a0003 | c0005 | t0005 | g0338 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01928 | hp1 | a0001 | c0003 | t0004 | g0307 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0306 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01952 | hp2 | a0001 | c0003 | t0006 | g0300 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02027 | hp2 | a0001 | c0002 | t0006 | g0243 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02056 | hp2 | a0001 | c0001 | t0012 | g0203 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0285 | EAS | CDX | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | CDX | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0178 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02523 | hp1 | a0001 | c0003 | t0002 | g0321 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02602 | hp1 | a0001 | c0003 | t0005 | g0332 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0249 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0230 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0094 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02735 | hp2 | a0007 | c0007 | t0005 | g0342 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02818 | hp2 | a0002 | c0004 | t0010 | g0136 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02897 | hp1 | a0001 | c0003 | t0007 | g0021 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0142 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0295 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03098 | hp1 | a0002 | c0004 | t0010 | g0138 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03130 | hp1 | a0002 | c0004 | t0010 | g0137 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03139 | hp2 | a0002 | c0004 | t0010 | g0135 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03209 | hp1 | a0002 | c0004 | t0013 | g0011 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0297 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0263 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0298 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0266 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03834 | hp1 | a0001 | c0002 | t0007 | g0253 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03942 | hp1 | a0001 | c0003 | t0005 | g0331 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0323 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04115 | hp1 | a0001 | c0003 | t0014 | g0303 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0122 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04199 | hp1 | a0001 | c0003 | t0006 | g0293 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0264 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0287 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18941 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18945 | hp2 | a0004 | c0008 | t0001 | g0027 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18950 | hp2 | a0001 | c0003 | t0006 | g0294 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18954 | hp1 | a0001 | c0002 | t0007 | g0238 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18959 | hp1 | a0001 | c0002 | t0007 | g0261 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18962 | hp2 | a0005 | c0006 | t0002 | g0233 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0288 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18967 | hp2 | a0001 | c0003 | t0003 | g0308 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0018 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18981 | hp1 | a0001 | c0003 | t0007 | g0284 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0281 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18989 | hp1 | a0005 | c0006 | t0002 | g0245 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19000 | hp2 | a0001 | c0001 | t0012 | g0207 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19001 | hp2 | a0001 | c0002 | t0006 | g0270 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0299 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19006 | hp1 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0296 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19056 | hp2 | a0001 | c0002 | t0007 | g0241 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0191 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19062 | hp2 | a0001 | c0002 | t0006 | g0218 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19063 | hp2 | a0001 | c0003 | t0002 | g0320 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19065 | hp2 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19066 | hp1 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19079 | hp1 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19083 | hp2 | a0001 | c0002 | t0006 | g0221 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0286 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ASW | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20805 | hp2 | a0004 | c0009 | t0001 | g0159 | EUR | TSI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01123 | hp1 | a0001 | c0003 | t0005 | g0334 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG06807 | hp1 | a0003 | c0005 | t0005 | g0336 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| homoSapiens | chm13v2 | a0003 | c0005 | t0005 | g0339 | REF | REF | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0087 | REF | REF | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53693919 | C | A | 1 | a0004 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.1334G>T | p.Arg445Leu | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1480/2226 | 1334/1557 | 445/518 | chr2 | 53693919 | |||
| chr2:53693920 | G | A | 1 | a0004 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1333C>T | p.Arg445Cys | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1479/2226 | 1333/1557 | 445/518 | chr2 | 53693920 | |||
| chr2:53694001 | T | C | 1 | a0005 | 2 | NA18962.hp2 NA18989.hp1 |
missense_variant | MODERATE | c.1252A>G | p.Ser418Gly | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1398/2226 | 1252/1557 | 418/518 | chr2 | 53694001 | |||
| chr2:53714544 | A | G | 1 | a0007 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.820T>C | p.Cys274Arg | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/10 | 966/2226 | 820/1557 | 274/518 | chr2 | 53714544 | |||
| chr2:53728730 | T | C | 1 | a0002 | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
missense_variant | MODERATE | c.586A>G | p.Ser196Gly | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 732/2226 | 586/1557 | 196/518 | chr2 | 53728730 | |||
| chr2:53728845 | T | A | 1 | a0003 | 3 | HG01106.hp2 HG01261.hp2 HG06807.hp1 |
missense_variant&splice_region_variant | MODERATE | c.471A>T | p.Glu157Asp | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 617/2226 | 471/1557 | 157/518 | chr2 | 53728845 | |||
| chr2:53765485 | G | C | 1 | a0006 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.88C>G | p.Leu30Val | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/10 | 234/2226 | 88/1557 | 30/518 | chr2 | 53765485 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53728713 | C | T | 3 | a0001c0003 a0003c0005 a0007c0007 |
49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
splice_region_variant&synonymous_variant | LOW | c.603G>A | p.Ser201Ser | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 749/2226 | 603/1557 | 201/518 | chr2 | 53728713 | |||
| chr2:53765456 | A | T | 2 | a0001c0002 a0005c0006 |
51 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
synonymous_variant | LOW | c.117T>A | p.Ala39Ala | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/10 | 263/2226 | 117/1557 | 39/518 | chr2 | 53765456 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53670114 | A | G | 2 | a0001c0001t0011 a0001c0003t0011 |
3 | HG00323.hp1 HG01256.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*389T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 389 | chr2 | 53670114 | ||||||
| chr2:53670130 | G | A | 1 | a0001c0003t0014 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 373 | chr2 | 53670130 | ||||||
| chr2:53670171 | A | G | 1 | a0001c0001t0015 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 332 | chr2 | 53670171 | ||||||
| chr2:53670292 | A | AT | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0002t0006 others(3): Show |
37 | HG00438.hp2 HG01074.hp1 HG01346.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*210dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 210 | chr2 | 53670292 | ||||||
| chr2:53670292 | AT | A | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(3): Show |
55 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*210delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 210 | chr2 | 53670292 | ||||||
| chr2:53670292 | ATT | A | 1 | a0001c0001t0008 | 8 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*209_*210delAA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 209 | chr2 | 53670292 | ||||||
| chr2:53670292 | ATTTTTTT | A | 4 | a0001c0001t0005 a0001c0003t0005 a0003c0005t0005 others(1): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*204_*210delAAAAAA others(1): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 204 | chr2 | 53670292 | ||||||
| chr2:53670388 | C | G | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(12): Show |
105 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 115 | chr2 | 53670388 | ||||||
| chr2:53670399 | A | G | 2 | a0002c0004t0010 a0002c0004t0013 |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 104 | chr2 | 53670399 | ||||||
| chr2:53670431 | G | A | 2 | a0001c0001t0009 a0001c0001t0012 |
7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*72C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 72 | chr2 | 53670431 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53670895 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(59): Show |
65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1370-205A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670895 | |||||||
| chr2:53670985 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-295A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670985 | |||||||
| chr2:53670986 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-296C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670986 | |||||||
| chr2:53671353 | C | CGT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0037 others(102): Show |
106 | HG00323.hp1 HG00423.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1370-665_1370-664d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | C | CGTGT | 73 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0029 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1370-667_1370-664d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | C | CGTGTGT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0209 a0001c0001t0002g0255 others(4): Show |
7 | HG01255.hp2 HG02015.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1370-669_1370-664d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0004g0271 a0001c0001t0004g0274 |
2 | HG01074.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1370-673_1370-664d others(12): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0273 a0001c0001t0004g0149 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1370-675_1370-664d others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | CGT | C | 58 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0062 others(55): Show |
60 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1370-665_1370-664d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | CGTGT | C | 15 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0143 others(12): Show |
15 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1370-667_1370-664d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | CGTGTGT | C | 5 | a0001c0001t0003g0217 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-669_1370-664d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1370-671_1370-664d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671353 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-677_1370-664d others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | |||||||
| chr2:53671514 | C | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1370-824G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671514 | |||||||
| chr2:53671531 | G | A | 3 | a0001c0003t0002g0309 a0001c0003t0002g0320 a0001c0003t0002g0321 |
3 | HG00621.hp2 HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1370-841C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671531 | |||||||
| chr2:53671633 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1370-943G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671633 | |||||||
| chr2:53671689 | GCGGAGGT others(18): Show |
G | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1024_1370-100 others(29): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671689 | |||||||
| chr2:53671691 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-1001C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671691 | |||||||
| chr2:53671695 | GTTGCAGT others(175): Show |
G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1187_1370-100 others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671695 | |||||||
| chr2:53671716 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1026C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671716 | |||||||
| chr2:53671718 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1028G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671718 | |||||||
| chr2:53671719 | ACT | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1031_1370-103 others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671719 | |||||||
| chr2:53671759 | C | CA | 10 | a0001c0001t0001g0014 a0001c0001t0003g0217 a0001c0001t0004g0013 others(7): Show |
10 | HG02258.hp1 HG02818.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1070dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671759 | |||||||
| chr2:53671853 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1370-1163G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671853 | |||||||
| chr2:53671880 | A | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1190T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671880 | |||||||
| chr2:53671884 | C | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1194G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671884 | |||||||
| chr2:53671885 | T | A | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1195A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671885 | |||||||
| chr2:53671886 | T | A | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1196A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671886 | |||||||
| chr2:53671888 | TATAAA | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1203_1370-119 others(9): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671888 | |||||||
| chr2:53671927 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0003g0042 a0001c0001t0003g0043 others(7): Show |
10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1237C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671927 | |||||||
| chr2:53671961 | C | T | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-1271G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671961 | |||||||
| chr2:53672301 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-1611G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672301 | |||||||
| chr2:53672451 | G | A | 1 | a0001c0003t0002g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1370-1761C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672451 | |||||||
| chr2:53672629 | A | G | 51 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(48): Show |
53 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1370-1939T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672629 | |||||||
| chr2:53672631 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1370-1941A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672631 | |||||||
| chr2:53672707 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(7): Show |
11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1370-2017T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672707 | |||||||
| chr2:53672741 | G | C | 2 | a0001c0002t0002g0242 a0001c0002t0006g0243 |
2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1370-2051C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672741 | |||||||
| chr2:53672781 | G | A | 6 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(3): Show |
6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-2091C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672781 | |||||||
| chr2:53672960 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1370-2270A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672960 | |||||||
| chr2:53673070 | A | G | 1 | a0001c0001t0004g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1370-2380T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673070 | |||||||
| chr2:53673101 | C | CA | 10 | a0001c0001t0001g0310 a0001c0001t0001g0319 a0001c0001t0001g0322 others(7): Show |
10 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-2412dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673101 | |||||||
| chr2:53673259 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-2569C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673259 | |||||||
| chr2:53673338 | G | A | 1 | a0001c0002t0002g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1370-2648C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673338 | |||||||
| chr2:53673434 | C | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0153 others(16): Show |
19 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1370-2744G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673434 | |||||||
| chr2:53673535 | G | C | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1370-2845C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673535 | |||||||
| chr2:53673634 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1370-2944A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673634 | |||||||
| chr2:53673664 | G | C | 6 | a0001c0001t0003g0217 a0002c0004t0010g0135 a0002c0004t0010g0136 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-2974C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673664 | |||||||
| chr2:53673743 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-3053A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673743 | |||||||
| chr2:53673815 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-3125A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673815 | |||||||
| chr2:53673878 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1370-3188A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673878 | |||||||
| chr2:53674340 | A | G | 52 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-3650T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674340 | |||||||
| chr2:53674642 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-3952C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674642 | |||||||
| chr2:53674760 | A | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1370-4070T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674760 | |||||||
| chr2:53674829 | C | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-4139G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674829 | |||||||
| chr2:53674836 | A | G | 212 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1370-4146T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674836 | |||||||
| chr2:53674844 | A | AAAATAAG others(8): Show |
1 | a0001c0001t0003g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4155_1370-415 others(19): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674844 | |||||||
| chr2:53674847 | A | ATAAGTAA others(3): Show |
1 | a0001c0001t0001g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4158_1370-415 others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674847 | |||||||
| chr2:53674848 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4158T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674848 | |||||||
| chr2:53674849 | G | A | 1 | a0001c0001t0003g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4159C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674849 | |||||||
| chr2:53674850 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4160G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674850 | |||||||
| chr2:53674850 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4160G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674850 | |||||||
| chr2:53674874 | C | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
221 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1370-4184G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674874 | |||||||
| chr2:53674983 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1370-4293G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674983 | |||||||
| chr2:53675029 | C | T | 213 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
217 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1370-4339G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675029 | |||||||
| chr2:53675038 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1370-4348A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675038 | |||||||
| chr2:53675090 | C | T | 52 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-4400G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675090 | |||||||
| chr2:53675226 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1370-4536A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675226 | |||||||
| chr2:53675337 | T | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4647A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675337 | |||||||
| chr2:53675342 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4652T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675342 | |||||||
| chr2:53675343 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4653T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675343 | |||||||
| chr2:53675345 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4655T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675345 | |||||||
| chr2:53675347 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4657T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675347 | |||||||
| chr2:53675348 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4658T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675348 | |||||||
| chr2:53675350 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4660T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675350 | |||||||
| chr2:53675352 | G | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4662C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675352 | |||||||
| chr2:53675353 | C | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4663G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675353 | |||||||
| chr2:53675356 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4666T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675356 | |||||||
| chr2:53675377 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4687A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675377 | |||||||
| chr2:53675384 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4694T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675384 | |||||||
| chr2:53675386 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4696A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675386 | |||||||
| chr2:53675387 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4697A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675387 | |||||||
| chr2:53675396 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4706T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675396 | |||||||
| chr2:53675399 | G | T | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1370-4709C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675399 | |||||||
| chr2:53675403 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4713T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675403 | |||||||
| chr2:53675416 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4726T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675416 | |||||||
| chr2:53675417 | T | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4727A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675417 | |||||||
| chr2:53675421 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4731T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675421 | |||||||
| chr2:53675423 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4733A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675423 | |||||||
| chr2:53675425 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4735A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675425 | |||||||
| chr2:53675427 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4737A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675427 | |||||||
| chr2:53675432 | A | C | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1370-4742T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675432 | |||||||
| chr2:53675434 | G | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4744C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675434 | |||||||
| chr2:53675435 | A | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4745T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675435 | |||||||
| chr2:53675437 | C | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4747G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675437 | |||||||
| chr2:53675438 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4748T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675438 | |||||||
| chr2:53675439 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4749T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675439 | |||||||
| chr2:53675442 | T | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4752A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675442 | |||||||
| chr2:53675447 | G | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4757C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675447 | |||||||
| chr2:53675456 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4766A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675456 | |||||||
| chr2:53675457 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4767A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675457 | |||||||
| chr2:53675462 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4772T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675462 | |||||||
| chr2:53675466 | A | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4776T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675466 | |||||||
| chr2:53675484 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4794T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675484 | |||||||
| chr2:53675485 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4795T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675485 | |||||||
| chr2:53675488 | C | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4798G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675488 | |||||||
| chr2:53675489 | A | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4799T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675489 | |||||||
| chr2:53675492 | G | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4802C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675492 | |||||||
| chr2:53675493 | A | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4803T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675493 | |||||||
| chr2:53675510 | G | T | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4820C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675510 | |||||||
| chr2:53675512 | T | G | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4822A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675512 | |||||||
| chr2:53675513 | T | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4823A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675513 | |||||||
| chr2:53675516 | T | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4826A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675516 | |||||||
| chr2:53675517 | C | A | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4827G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675517 | |||||||
| chr2:53675519 | G | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4829C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675519 | |||||||
| chr2:53675707 | T | A | 1 | a0001c0001t0004g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1370-5017A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675707 | |||||||
| chr2:53675787 | T | C | 6 | a0001c0002t0002g0237 a0001c0002t0002g0256 a0001c0002t0002g0258 others(3): Show |
6 | NA18952.hp2 NA18954.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-5097A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675787 | |||||||
| chr2:53675890 | T | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-5200A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675890 | |||||||
| chr2:53676024 | A | G | 196 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(193): Show |
199 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1370-5334T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676024 | |||||||
| chr2:53676051 | T | A | 1 | a0001c0001t0007g0022 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1370-5361A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676051 | |||||||
| chr2:53676161 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-5471T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676161 | |||||||
| chr2:53676371 | T | C | 9 | a0001c0003t0002g0289 a0001c0003t0002g0290 a0001c0003t0002g0291 others(6): Show |
9 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1370-5681A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676371 | |||||||
| chr2:53676407 | T | C | 4 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0153 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-5717A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676407 | |||||||
| chr2:53676608 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1370-5918G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676608 | |||||||
| chr2:53676672 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1370-5982A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676672 | |||||||
| chr2:53676730 | T | A | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1370-6040A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676730 | |||||||
| chr2:53677218 | T | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-6528A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677218 | |||||||
| chr2:53677356 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-6666G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677356 | |||||||
| chr2:53677388 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1370-6698G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677388 | |||||||
| chr2:53677390 | C | T | 1 | a0001c0003t0002g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1370-6700G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677390 | |||||||
| chr2:53677487 | GT | G | 13 | a0001c0001t0001g0035 a0001c0001t0005g0003 a0001c0003t0005g0311 others(10): Show |
14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1370-6798delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677487 | |||||||
| chr2:53677495 | T | A | 87 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(84): Show |
87 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1370-6805A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677495 | |||||||
| chr2:53677496 | A | T | 71 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0152 others(68): Show |
73 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1370-6806T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677496 | |||||||
| chr2:53677624 | T | C | 11 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(8): Show |
11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1370-6934A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677624 | |||||||
| chr2:53677671 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-6981T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677671 | |||||||
| chr2:53677694 | G | A | 1 | a0001c0002t0001g0257 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1370-7004C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677694 | |||||||
| chr2:53677721 | T | G | 52 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-7031A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677721 | |||||||
| chr2:53677830 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-7140A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677830 | |||||||
| chr2:53677938 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1370-7248A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677938 | |||||||
| chr2:53677994 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1370-7304A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677994 | |||||||
| chr2:53678140 | GGT | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(332): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1370-7452_1370-745 others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678140 | |||||||
| chr2:53678161 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1370-7471T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678161 | |||||||
| chr2:53678174 | A | C | 59 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0152 others(56): Show |
61 | HG00408.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1370-7484T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678174 | |||||||
| chr2:53678188 | G | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-7498C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678188 | |||||||
| chr2:53678357 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0190 a0001c0001t0003g0117 |
3 | HG02886.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1370-7667G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678357 | |||||||
| chr2:53678394 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0079 a0001c0001t0004g0080 |
3 | NA18943.hp1 NA18987.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1370-7704A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678394 | |||||||
| chr2:53678706 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0004g0156 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1370-8016C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678706 | |||||||
| chr2:53679219 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1370-8529A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679219 | |||||||
| chr2:53679239 | C | T | 2 | a0001c0002t0002g0242 a0001c0002t0006g0243 |
2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1370-8549G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679239 | |||||||
| chr2:53679261 | C | A | 4 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-8571G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679261 | |||||||
| chr2:53679291 | T | C | 1 | a0001c0003t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1370-8601A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679291 | |||||||
| chr2:53679321 | T | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0210 others(18): Show |
21 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1370-8631A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679321 | |||||||
| chr2:53679373 | A | G | 1 | a0001c0002t0002g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1370-8683T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679373 | |||||||
| chr2:53679384 | C | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0210 a0001c0001t0001g0215 others(11): Show |
14 | HG01074.hp1 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1370-8694G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679384 | |||||||
| chr2:53679406 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0003g0042 others(7): Show |
10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-8716C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679406 | |||||||
| chr2:53679416 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-8726G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679416 | |||||||
| chr2:53679457 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1370-8767A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679457 | |||||||
| chr2:53679573 | A | G | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1370-8883T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679573 | |||||||
| chr2:53679593 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1370-8903C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679593 | |||||||
| chr2:53679702 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1370-9012T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679702 | |||||||
| chr2:53679741 | A | G | 10 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(7): Show |
10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370-9051T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679741 | |||||||
| chr2:53679781 | G | T | 4 | a0001c0001t0008g0034 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-9091C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679781 | |||||||
| chr2:53679798 | A | G | 193 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(190): Show |
196 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1370-9108T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679798 | |||||||
| chr2:53679834 | T | C | 10 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370-9144A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679834 | |||||||
| chr2:53679940 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1370-9250C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679940 | |||||||
| chr2:53679978 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1370-9288C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679978 | |||||||
| chr2:53680026 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-9336C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680026 | |||||||
| chr2:53680131 | A | T | 44 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(41): Show |
46 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1370-9441T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680131 | |||||||
| chr2:53680238 | C | A | 1 | a0001c0001t0009g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1370-9548G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680238 | |||||||
| chr2:53680424 | T | A | 5 | a0001c0001t0001g0150 a0001c0001t0003g0145 a0001c0001t0003g0146 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-9734A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680424 | |||||||
| chr2:53680460 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1370-9770A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680460 | |||||||
| chr2:53680495 | G | C | 110 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(107): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1370-9805C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680495 | |||||||
| chr2:53680637 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0003g0042 others(7): Show |
10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-9947A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680637 | |||||||
| chr2:53680694 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-10004A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680694 | |||||||
| chr2:53680737 | A | T | 4 | a0001c0002t0002g0231 a0001c0002t0002g0232 a0001c0002t0002g0235 others(1): Show |
4 | HG00673.hp1 HG02040.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-10047T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680737 | |||||||
| chr2:53680738 | T | C | 124 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0267 others(121): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1370-10048A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680738 | |||||||
| chr2:53680884 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-10194G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680884 | |||||||
| chr2:53680921 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1370-10231C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680921 | |||||||
| chr2:53681254 | T | C | 338 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(335): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1370-10564A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681254 | |||||||
| chr2:53681289 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1370-10599G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681289 | |||||||
| chr2:53681360 | A | C | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0126 |
3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1370-10670T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681360 | |||||||
| chr2:53681505 | C | G | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(185): Show |
191 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1370-10815G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681505 | |||||||
| chr2:53681736 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1370-11046C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681736 | |||||||
| chr2:53681886 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0148 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-11196C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681886 | |||||||
| chr2:53681918 | G | T | 9 | a0001c0001t0002g0061 a0001c0002t0002g0219 a0001c0002t0002g0222 others(6): Show |
9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11228C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681918 | |||||||
| chr2:53681919 | G | A | 9 | a0001c0001t0002g0061 a0001c0002t0002g0219 a0001c0002t0002g0222 others(6): Show |
9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11229C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681919 | |||||||
| chr2:53681926 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1370-11236C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681926 | |||||||
| chr2:53681953 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1370-11263A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681953 | |||||||
| chr2:53682063 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-11373C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682063 | |||||||
| chr2:53682157 | C | T | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1370-11467G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682157 | |||||||
| chr2:53682159 | C | CA | 52 | a0001c0001t0001g0083 a0001c0001t0001g0127 a0001c0001t0001g0150 others(49): Show |
53 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1370-11470dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682159 | |||||||
| chr2:53682218 | G | C | 12 | a0001c0001t0005g0003 a0001c0003t0005g0311 a0001c0003t0005g0328 others(9): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1370-11528C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682218 | |||||||
| chr2:53682224 | T | G | 9 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11534A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682224 | |||||||
| chr2:53682238 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1370-11548A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682238 | |||||||
| chr2:53682280 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1370-11590T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682280 | |||||||
| chr2:53682307 | A | G | 200 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(197): Show |
204 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1369+11577T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682307 | |||||||
| chr2:53682540 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1369+11344C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682540 | |||||||
| chr2:53682783 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0003g0171 a0001c0001t0003g0179 others(1): Show |
4 | HG00621.hp1 HG02080.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+11101G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682783 | |||||||
| chr2:53682816 | T | C | 76 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0150 others(73): Show |
78 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1369+11068A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682816 | |||||||
| chr2:53682926 | G | A | 11 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(8): Show |
11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10958C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682926 | |||||||
| chr2:53682947 | C | A | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1369+10937G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682947 | |||||||
| chr2:53683021 | T | C | 118 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0056 others(115): Show |
119 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1369+10863A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683021 | |||||||
| chr2:53683110 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+10774C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683110 | |||||||
| chr2:53683132 | C | G | 10 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(7): Show |
10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+10752G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683132 | |||||||
| chr2:53683257 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0134 |
2 | NA18962.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1369+10627G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683257 | |||||||
| chr2:53683261 | C | T | 9 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(6): Show |
9 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+10623G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683261 | |||||||
| chr2:53683335 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0003g0042 others(8): Show |
11 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10549T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683335 | |||||||
| chr2:53683336 | TCTTTTAA others(3): Show |
T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0003g0042 others(8): Show |
11 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10538_1369+10 others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683336 | |||||||
| chr2:53683394 | T | A | 1 | a0001c0001t0009g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1369+10490A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683394 | |||||||
| chr2:53683414 | T | TG | 8 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG02080.hp2 HG02818.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1369+10469dupC | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683414 | |||||||
| chr2:53683415 | G | GT | 16 | a0001c0001t0001g0128 a0001c0001t0001g0310 a0001c0001t0001g0318 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369+10468dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683415 | |||||||
| chr2:53683416 | T | G | 48 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0175 others(45): Show |
50 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1369+10468A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683416 | |||||||
| chr2:53683659 | T | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1369+10225A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683659 | |||||||
| chr2:53683971 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1369+9913A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683971 | |||||||
| chr2:53683997 | C | T | 50 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(47): Show |
52 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1369+9887G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683997 | |||||||
| chr2:53684111 | A | G | 1 | a0001c0003t0005g0343 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1369+9773T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684111 | |||||||
| chr2:53684151 | T | C | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1369+9733A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684151 | |||||||
| chr2:53684300 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0341 |
2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1369+9584A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684300 | |||||||
| chr2:53684324 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1369+9560A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684324 | |||||||
| chr2:53684447 | G | T | 4 | a0001c0001t0003g0177 a0001c0001t0003g0195 a0001c0001t0003g0197 others(1): Show |
4 | NA18955.hp1 NA18967.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+9437C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684447 | |||||||
| chr2:53684452 | C | T | 2 | a0001c0002t0002g0242 a0001c0002t0006g0243 |
2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1369+9432G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684452 | |||||||
| chr2:53684482 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1369+9402T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684482 | |||||||
| chr2:53684583 | A | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+9301T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684583 | |||||||
| chr2:53684612 | T | C | 1 | a0001c0002t0002g0222 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1369+9272A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684612 | |||||||
| chr2:53684676 | G | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1369+9208C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684676 | |||||||
| chr2:53684832 | A | T | 1 | a0001c0002t0002g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1369+9052T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684832 | |||||||
| chr2:53684845 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0154 others(18): Show |
22 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1369+9039T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684845 | |||||||
| chr2:53684991 | G | A | 10 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(7): Show |
10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+8893C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684991 | |||||||
| chr2:53685120 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369+8764C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685120 | |||||||
| chr2:53685136 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02080.hp2 NA18968.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+8748A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685136 | |||||||
| chr2:53685202 | A | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(57): Show |
63 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1369+8682T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685202 | |||||||
| chr2:53685414 | G | A | 1 | a0001c0003t0011g0329 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1369+8470C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685414 | |||||||
| chr2:53685424 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1369+8460T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685424 | |||||||
| chr2:53685648 | T | A | 1 | a0001c0002t0006g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1369+8236A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685648 | |||||||
| chr2:53685727 | A | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+8157T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685727 | |||||||
| chr2:53685975 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+7909T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685975 | |||||||
| chr2:53686068 | G | A | 1 | a0001c0003t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1369+7816C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686068 | |||||||
| chr2:53686279 | T | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0001g0089 |
3 | HG01074.hp2 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1369+7605A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686279 | |||||||
| chr2:53686472 | C | A | 44 | a0001c0001t0005g0003 a0001c0003t0002g0020 a0001c0003t0002g0277 others(41): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1369+7412G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686472 | |||||||
| chr2:53686593 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+7291T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686593 | |||||||
| chr2:53686662 | TA | T | 164 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0152 others(161): Show |
167 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1369+7221delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686662 | |||||||
| chr2:53686759 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1369+7125G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686759 | |||||||
| chr2:53686816 | G | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0322 |
2 | HG00408.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1369+7068C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686816 | |||||||
| chr2:53686866 | C | T | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1369+7018G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686866 | |||||||
| chr2:53687008 | T | C | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369+6876A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687008 | |||||||
| chr2:53687024 | G | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1369+6860C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687024 | |||||||
| chr2:53687038 | G | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+6846C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687038 | |||||||
| chr2:53687105 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+6779G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687105 | |||||||
| chr2:53687258 | A | C | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1369+6626T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687258 | |||||||
| chr2:53687262 | A | T | 51 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0170 others(48): Show |
53 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1369+6622T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687262 | |||||||
| chr2:53687462 | G | C | 5 | a0001c0001t0001g0150 a0001c0001t0003g0145 a0001c0001t0003g0146 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+6422C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687462 | |||||||
| chr2:53687521 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+6363C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687521 | |||||||
| chr2:53687624 | C | A | 1 | a0001c0001t0008g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1369+6260G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687624 | |||||||
| chr2:53687924 | T | C | 55 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(52): Show |
55 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1369+5960A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687924 | |||||||
| chr2:53687971 | C | T | 1 | a0001c0002t0002g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1369+5913G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687971 | |||||||
| chr2:53687986 | T | G | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1369+5898A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687986 | |||||||
| chr2:53688174 | G | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0154 others(14): Show |
18 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1369+5710C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688174 | |||||||
| chr2:53688223 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0003g0205 |
2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1369+5661G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688223 | |||||||
| chr2:53688282 | G | A | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1369+5602C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688282 | |||||||
| chr2:53688300 | C | T | 99 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(96): Show |
100 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1369+5584G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688300 | |||||||
| chr2:53688318 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0154 others(14): Show |
18 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1369+5566C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688318 | |||||||
| chr2:53688460 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1369+5424C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688460 | |||||||
| chr2:53688726 | T | C | 106 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0139 others(103): Show |
107 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1369+5158A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688726 | |||||||
| chr2:53688808 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1369+5076A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688808 | |||||||
| chr2:53689033 | A | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0001t0001g0134 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+4851T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689033 | |||||||
| chr2:53689082 | T | G | 2 | a0001c0003t0002g0320 a0001c0003t0002g0321 |
2 | HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1369+4802A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689082 | |||||||
| chr2:53689526 | C | G | 7 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(4): Show |
7 | HG01074.hp1 HG01261.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1369+4358G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689526 | |||||||
| chr2:53689534 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+4350A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689534 | |||||||
| chr2:53689658 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1369+4226A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689658 | |||||||
| chr2:53689712 | G | C | 117 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(114): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1369+4172C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689712 | |||||||
| chr2:53689811 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1369+4073C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689811 | |||||||
| chr2:53689839 | TA | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1369+4044delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689839 | |||||||
| chr2:53689936 | T | C | 15 | a0001c0001t0001g0150 a0001c0001t0001g0210 a0001c0001t0001g0215 others(12): Show |
15 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1369+3948A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689936 | |||||||
| chr2:53689989 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0003g0042 a0001c0001t0003g0043 others(7): Show |
10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+3895A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689989 | |||||||
| chr2:53690044 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1369+3840G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690044 | |||||||
| chr2:53690057 | G | A | 1 | a0001c0003t0002g0280 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1369+3827C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690057 | |||||||
| chr2:53690105 | A | G | 2 | a0002c0004t0010g0135 a0002c0004t0013g0011 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1369+3779T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690105 | |||||||
| chr2:53690217 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1369+3667G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690217 | |||||||
| chr2:53690251 | A | T | 10 | a0001c0001t0001g0150 a0001c0001t0003g0145 a0001c0001t0003g0146 others(7): Show |
10 | HG00323.hp1 HG01256.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+3633T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690251 | |||||||
| chr2:53690255 | T | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(183): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1369+3629A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690255 | |||||||
| chr2:53690259 | T | A | 28 | a0001c0001t0001g0097 a0001c0001t0001g0133 a0001c0001t0001g0209 others(25): Show |
28 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1369+3625A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690259 | |||||||
| chr2:53690292 | A | G | 2 | a0001c0001t0008g0033 a0001c0001t0008g0034 |
2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1369+3592T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690292 | |||||||
| chr2:53690389 | G | C | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1369+3495C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690389 | |||||||
| chr2:53690529 | C | T | 99 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(96): Show |
100 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1369+3355G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690529 | |||||||
| chr2:53690560 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1369+3324C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690560 | |||||||
| chr2:53690623 | G | GT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(60): Show |
66 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1369+3260dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690623 | |||||||
| chr2:53690664 | C | T | 99 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(96): Show |
100 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1369+3220G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690664 | |||||||
| chr2:53690684 | T | G | 10 | a0001c0001t0001g0015 a0001c0001t0003g0042 a0001c0001t0003g0043 others(7): Show |
10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+3200A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690684 | |||||||
| chr2:53690883 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1369+3001G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690883 | |||||||
| chr2:53690969 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1369+2915T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690969 | |||||||
| chr2:53691108 | C | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(280): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1369+2776G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691108 | |||||||
| chr2:53691110 | A | C | 6 | a0001c0001t0001g0014 a0001c0001t0002g0139 a0001c0001t0002g0141 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369+2774T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691110 | |||||||
| chr2:53691262 | G | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1369+2622C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691262 | |||||||
| chr2:53691304 | G | A | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1369+2580C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691304 | |||||||
| chr2:53691353 | A | G | 10 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+2531T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691353 | |||||||
| chr2:53691466 | G | A | 1 | a0001c0001t0004g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1369+2418C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691466 | |||||||
| chr2:53691751 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+2133G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691751 | |||||||
| chr2:53691805 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+2079G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691805 | |||||||
| chr2:53692021 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1369+1863A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692021 | |||||||
| chr2:53692083 | C | G | 3 | a0001c0003t0002g0285 a0001c0003t0002g0287 a0001c0003t0002g0288 |
3 | HG02155.hp1 NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1369+1801G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692083 | |||||||
| chr2:53692210 | G | A | 52 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0002t0002g0016 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1369+1674C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692210 | |||||||
| chr2:53692485 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1369+1399T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692485 | |||||||
| chr2:53692526 | C | G | 1 | a0001c0001t0002g0061 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1369+1358G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692526 | |||||||
| chr2:53692630 | C | T | 10 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+1254G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692630 | |||||||
| chr2:53692631 | T | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0267 others(22): Show |
25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1369+1253A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692631 | |||||||
| chr2:53692646 | G | C | 1 | a0001c0002t0002g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1369+1238C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692646 | |||||||
| chr2:53693214 | G | C | 1 | a0001c0001t0004g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1369+670C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693214 | |||||||
| chr2:53693256 | G | T | 1 | a0001c0003t0005g0311 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1369+628C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693256 | |||||||
| chr2:53693457 | G | A | 7 | a0001c0001t0001g0105 a0001c0001t0008g0028 a0001c0001t0008g0030 others(4): Show |
7 | HG01255.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1369+427C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693457 | |||||||
| chr2:53693721 | A | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+163T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693721 | |||||||
| chr2:53693793 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1369+91G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693793 | |||||||
| chr2:53693794 | G | A | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(170): Show |
176 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1369+90C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693794 | |||||||
| chr2:53693833 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1369+51T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693833 | |||||||
| chr2:53694133 | C | T | 99 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0227 others(96): Show |
100 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1239-119G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694133 | |||||||
| chr2:53694157 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(4): Show |
7 | HG01074.hp1 HG01261.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-143T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694157 | |||||||
| chr2:53694184 | C | G | 16 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(13): Show |
16 | HG01074.hp1 HG01167.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1239-170G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694184 | |||||||
| chr2:53694617 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0201 |
2 | HG00733.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1239-603C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694617 | |||||||
| chr2:53694646 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(59): Show |
65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1239-632T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694646 | |||||||
| chr2:53694694 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1239-680A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694694 | |||||||
| chr2:53694754 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(59): Show |
65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1239-740T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694754 | |||||||
| chr2:53694800 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1239-786A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694800 | |||||||
| chr2:53694849 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-835A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694849 | |||||||
| chr2:53694884 | C | T | 208 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(205): Show |
212 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1239-870G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694884 | |||||||
| chr2:53694900 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(7): Show |
11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239-886G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694900 | |||||||
| chr2:53694987 | G | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0085 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1239-973C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694987 | |||||||
| chr2:53695119 | G | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1239-1105C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695119 | |||||||
| chr2:53695134 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1239-1120C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695134 | |||||||
| chr2:53695188 | C | T | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-1174G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695188 | |||||||
| chr2:53695319 | C | T | 209 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
213 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1239-1305G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695319 | |||||||
| chr2:53695433 | T | C | 10 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1239-1419A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695433 | |||||||
| chr2:53695451 | G | C | 1 | a0001c0002t0002g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1239-1437C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695451 | |||||||
| chr2:53695651 | ATAATGCC others(2): Show |
A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(22): Show |
25 | HG00738.hp1 HG01074.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1239-1646_1239-163 others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695651 | |||||||
| chr2:53695688 | A | T | 221 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(218): Show |
225 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1239-1674T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695688 | |||||||
| chr2:53695702 | T | C | 1 | a0001c0003t0006g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239-1688A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695702 | |||||||
| chr2:53695738 | T | C | 1 | a0001c0002t0002g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1239-1724A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695738 | |||||||
| chr2:53695801 | G | A | 1 | a0001c0001t0008g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1239-1787C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695801 | |||||||
| chr2:53695806 | C | G | 211 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
215 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1239-1792G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695806 | |||||||
| chr2:53695911 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1239-1897A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695911 | |||||||
| chr2:53695993 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-1979A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695993 | |||||||
| chr2:53696047 | A | T | 1 | a0001c0002t0002g0237 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1239-2033T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696047 | |||||||
| chr2:53696078 | T | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0152 others(58): Show |
64 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1239-2064A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696078 | |||||||
| chr2:53696136 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239-2122A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696136 | |||||||
| chr2:53696315 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1239-2301G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696315 | |||||||
| chr2:53696340 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1239-2326G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696340 | |||||||
| chr2:53696354 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239-2340G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696354 | |||||||
| chr2:53696384 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 others(4): Show |
7 | HG02258.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-2370C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696384 | |||||||
| chr2:53696450 | TA | T | 8 | a0001c0001t0001g0162 a0001c0001t0001g0318 a0001c0001t0004g0161 others(5): Show |
8 | NA18973.hp2 NA18975.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1239-2437delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696450 | |||||||
| chr2:53696546 | G | C | 1 | a0001c0001t0003g0182 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1239-2532C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696546 | |||||||
| chr2:53696639 | T | C | 4 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0153 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-2625A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696639 | |||||||
| chr2:53696647 | T | C | 1 | a0001c0003t0002g0277 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1239-2633A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696647 | |||||||
| chr2:53696763 | C | T | 1 | a0001c0003t0006g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239-2749G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696763 | |||||||
| chr2:53696784 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0004g0026 a0004c0008t0001g0027 |
3 | NA18945.hp2 NA18955.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1239-2770A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696784 | |||||||
| chr2:53696816 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1239-2802A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696816 | |||||||
| chr2:53696817 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0072 others(4): Show |
7 | NA18959.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2803C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696817 | |||||||
| chr2:53696879 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0004g0149 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1239-2865C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696879 | |||||||
| chr2:53697167 | C | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1238+3104G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697167 | |||||||
| chr2:53697286 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
93 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1238+2985A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697286 | |||||||
| chr2:53697458 | GC | G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(52): Show |
55 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1238+2812delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697458 | |||||||
| chr2:53697560 | A | C | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1238+2711T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697560 | |||||||
| chr2:53697591 | C | G | 50 | a0001c0001t0003g0340 a0001c0003t0001g0304 a0001c0003t0001g0305 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1238+2680G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697591 | |||||||
| chr2:53697864 | C | G | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1238+2407G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697864 | |||||||
| chr2:53697879 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1238+2392G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697879 | |||||||
| chr2:53697950 | GTCTCAAT others(7): Show |
G | 1 | a0001c0002t0002g0222 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1238+2307_1238+232 others(18): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697950 | |||||||
| chr2:53698198 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+2073G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698198 | |||||||
| chr2:53698261 | T | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1238+2010A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698261 | |||||||
| chr2:53698359 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1238+1912G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698359 | |||||||
| chr2:53698514 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1238+1757G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698514 | |||||||
| chr2:53698557 | C | A | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0126 |
3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1238+1714G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698557 | |||||||
| chr2:53698623 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1238+1648G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698623 | |||||||
| chr2:53699030 | T | A | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238+1241A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699030 | |||||||
| chr2:53699145 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1238+1126G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699145 | |||||||
| chr2:53699166 | T | C | 222 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
225 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1238+1105A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699166 | |||||||
| chr2:53699416 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238+855G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699416 | |||||||
| chr2:53699426 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1238+845A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699426 | |||||||
| chr2:53699441 | G | A | 5 | a0001c0003t0002g0289 a0001c0003t0002g0291 a0001c0003t0002g0292 others(2): Show |
5 | HG00438.hp1 HG02074.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238+830C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699441 | |||||||
| chr2:53699495 | A | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0154 others(16): Show |
20 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1238+776T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699495 | |||||||
| chr2:53699650 | C | CAA | 77 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(74): Show |
79 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1238+619_1238+620d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699650 | |||||||
| chr2:53699739 | GC | G | 61 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(58): Show |
63 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1238+531delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699739 | |||||||
| chr2:53699769 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1238+502A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699769 | |||||||
| chr2:53700175 | A | C | 1 | a0001c0002t0002g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1238+96T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700175 | |||||||
| chr2:53700176 | T | TAC | 65 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(62): Show |
67 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1238+93_1238+94dup others(2): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700176 | |||||||
| chr2:53700233 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1238+38A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700233 | |||||||
| chr2:53700551 | A | C | 1 | a0001c0001t0008g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981-23T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700551 | |||||||
| chr2:53700629 | T | C | 2 | a0001c0003t0002g0278 a0001c0003t0002g0299 |
2 | NA19002.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.981-101A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700629 | |||||||
| chr2:53700711 | C | T | 1 | a0001c0002t0006g0221 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.981-183G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700711 | |||||||
| chr2:53700786 | T | TA | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-259dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700786 | |||||||
| chr2:53700795 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.981-267A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700795 | |||||||
| chr2:53701003 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-475A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701003 | |||||||
| chr2:53701005 | T | C | 1 | a0001c0003t0002g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.981-477A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701005 | |||||||
| chr2:53701129 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
25 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.981-601T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701129 | |||||||
| chr2:53701182 | C | T | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-654G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701182 | |||||||
| chr2:53701220 | C | T | 8 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-692G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701220 | |||||||
| chr2:53701245 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-717G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701245 | |||||||
| chr2:53701288 | T | A | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.981-760A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701288 | |||||||
| chr2:53701299 | T | C | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.981-771A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701299 | |||||||
| chr2:53701328 | C | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(60): Show |
63 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.981-800G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701328 | |||||||
| chr2:53701367 | T | C | 1 | a0001c0001t0004g0025 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.981-839A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701367 | |||||||
| chr2:53701442 | T | C | 9 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.981-914A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701442 | |||||||
| chr2:53701501 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0154 others(15): Show |
19 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.981-973C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701501 | |||||||
| chr2:53701587 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-1059A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701587 | |||||||
| chr2:53701898 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.981-1370G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701898 | |||||||
| chr2:53701975 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-1447G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701975 | |||||||
| chr2:53702054 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.981-1526G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702054 | |||||||
| chr2:53702079 | A | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-1551T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702079 | |||||||
| chr2:53702275 | G | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0003g0145 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-1747C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702275 | |||||||
| chr2:53702279 | C | T | 49 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(46): Show |
49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.981-1751G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702279 | |||||||
| chr2:53702409 | C | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0056 others(11): Show |
14 | HG02132.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.981-1881G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702409 | |||||||
| chr2:53702436 | ATGGATAA others(4): Show |
A | 1 | a0001c0003t0002g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.981-1919_981-1909d others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702436 | |||||||
| chr2:53702492 | A | C | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.981-1964T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702492 | |||||||
| chr2:53702542 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.981-2014G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702542 | |||||||
| chr2:53702549 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-2021A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702549 | |||||||
| chr2:53702718 | C | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
109 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.981-2190G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702718 | |||||||
| chr2:53702769 | A | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-2241T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702769 | |||||||
| chr2:53703457 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0134 |
2 | NA18962.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.981-2929T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703457 | |||||||
| chr2:53703460 | A | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-2932T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703460 | |||||||
| chr2:53703484 | G | A | 49 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(46): Show |
49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.981-2956C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703484 | |||||||
| chr2:53703543 | G | A | 1 | a0001c0003t0002g0290 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981-3015C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703543 | |||||||
| chr2:53703546 | C | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-3018G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703546 | |||||||
| chr2:53703682 | T | C | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.981-3154A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703682 | |||||||
| chr2:53703712 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.981-3184G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703712 | |||||||
| chr2:53703717 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.981-3189C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703717 | |||||||
| chr2:53703927 | C | T | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.981-3399G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703927 | |||||||
| chr2:53704053 | G | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(108): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.981-3525C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704053 | |||||||
| chr2:53704082 | G | C | 3 | a0001c0001t0003g0177 a0001c0001t0003g0195 a0001c0001t0003g0197 |
3 | NA18955.hp1 NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.981-3554C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704082 | |||||||
| chr2:53704088 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.981-3560C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704088 | |||||||
| chr2:53704142 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-3614G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704142 | |||||||
| chr2:53704339 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-3811G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704339 | |||||||
| chr2:53704359 | C | CA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0035 others(50): Show |
54 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.981-3832dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | |||||||
| chr2:53704359 | CA | C | 116 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.981-3832delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | |||||||
| chr2:53704359 | CAA | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(23): Show |
26 | HG00738.hp1 HG01169.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.981-3833_981-3832d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | |||||||
| chr2:53704359 | CAAA | C | 53 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(50): Show |
55 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.981-3834_981-3832d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | |||||||
| chr2:53704393 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.981-3865A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704393 | |||||||
| chr2:53704425 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-3897T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704425 | |||||||
| chr2:53704488 | G | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.981-3960C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704488 | |||||||
| chr2:53704791 | A | T | 1 | a0001c0003t0002g0309 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.981-4263T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704791 | |||||||
| chr2:53704869 | C | T | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.981-4341G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704869 | |||||||
| chr2:53704871 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0003g0202 |
2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.981-4343G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704871 | |||||||
| chr2:53704969 | A | G | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.981-4441T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704969 | |||||||
| chr2:53704997 | G | C | 50 | a0001c0001t0003g0340 a0001c0003t0001g0304 a0001c0003t0001g0305 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.981-4469C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704997 | |||||||
| chr2:53705295 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.981-4767C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705295 | |||||||
| chr2:53705310 | C | T | 2 | a0001c0002t0002g0242 a0001c0002t0006g0243 |
2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981-4782G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705310 | |||||||
| chr2:53705361 | C | A | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.981-4833G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705361 | |||||||
| chr2:53705532 | T | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.981-5004A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705532 | |||||||
| chr2:53705705 | T | A | 3 | a0001c0001t0001g0119 a0001c0001t0004g0026 a0004c0008t0001g0027 |
3 | NA18945.hp2 NA18955.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.981-5177A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705705 | |||||||
| chr2:53705934 | T | A | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5406A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705934 | |||||||
| chr2:53705943 | C | G | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5415G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705943 | |||||||
| chr2:53705947 | T | C | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5419A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705947 | |||||||
| chr2:53705949 | C | T | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5421G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705949 | |||||||
| chr2:53705951 | G | T | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5423C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705951 | |||||||
| chr2:53705979 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-5451A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705979 | |||||||
| chr2:53706015 | T | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-5487A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706015 | |||||||
| chr2:53706163 | A | G | 15 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(12): Show |
15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5635T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706163 | |||||||
| chr2:53706208 | G | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-5680C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706208 | |||||||
| chr2:53706301 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981-5773T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706301 | |||||||
| chr2:53706653 | G | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-6125C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706653 | |||||||
| chr2:53706686 | C | A | 69 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
72 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.981-6158G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706686 | |||||||
| chr2:53706769 | T | A | 1 | a0001c0001t0002g0228 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.981-6241A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706769 | |||||||
| chr2:53706887 | A | C | 16 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.981-6359T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706887 | |||||||
| chr2:53706944 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.981-6416G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706944 | |||||||
| chr2:53706957 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981-6429C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706957 | |||||||
| chr2:53707014 | C | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
95 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.981-6486G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707014 | |||||||
| chr2:53707023 | T | A | 4 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0153 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-6495A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707023 | |||||||
| chr2:53707191 | C | G | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-6663G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707191 | |||||||
| chr2:53707201 | A | C | 1 | a0001c0001t0002g0130 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.981-6673T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707201 | |||||||
| chr2:53707405 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.981-6877C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707405 | |||||||
| chr2:53707646 | C | CA | 77 | a0001c0001t0001g0005 a0001c0001t0001g0106 a0001c0001t0001g0148 others(74): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.980+6737dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707646 | |||||||
| chr2:53707698 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0096 |
2 | HG03490.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.980+6686G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707698 | |||||||
| chr2:53707767 | G | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+6617C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707767 | |||||||
| chr2:53707961 | C | CA | 12 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0090 others(9): Show |
12 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.980+6422dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707961 | |||||||
| chr2:53707961 | CA | C | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0140 others(178): Show |
183 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.980+6422delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707961 | |||||||
| chr2:53707974 | A | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0003g0145 others(4): Show |
7 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.980+6410T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707974 | |||||||
| chr2:53708126 | G | A | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+6258C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708126 | |||||||
| chr2:53708131 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+6253G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708131 | |||||||
| chr2:53708222 | G | GT | 7 | a0001c0001t0009g0178 a0001c0001t0009g0191 a0001c0001t0009g0198 others(4): Show |
7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+6161dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708222 | |||||||
| chr2:53708243 | C | T | 4 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6141G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708243 | |||||||
| chr2:53708363 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+6021A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708363 | |||||||
| chr2:53708381 | T | C | 1 | a0001c0001t0004g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.980+6003A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708381 | |||||||
| chr2:53708388 | A | G | 16 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+5996T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708388 | |||||||
| chr2:53708596 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.980+5788C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708596 | |||||||
| chr2:53708618 | A | G | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5766T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708618 | |||||||
| chr2:53708665 | A | C | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5719T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708665 | |||||||
| chr2:53708990 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.980+5394A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708990 | |||||||
| chr2:53708992 | T | C | 6 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(3): Show |
6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+5392A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708992 | |||||||
| chr2:53709099 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5285A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709099 | |||||||
| chr2:53709116 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.980+5268C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709116 | |||||||
| chr2:53709123 | T | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.980+5261A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709123 | |||||||
| chr2:53709320 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(7): Show |
11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+5064C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709320 | |||||||
| chr2:53709359 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(54): Show |
57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.980+5025C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709359 | |||||||
| chr2:53709416 | A | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.980+4968T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709416 | |||||||
| chr2:53709440 | T | G | 16 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+4944A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709440 | |||||||
| chr2:53709671 | A | G | 16 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+4713T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709671 | |||||||
| chr2:53709729 | G | C | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.980+4655C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709729 | |||||||
| chr2:53709734 | C | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+4650G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709734 | |||||||
| chr2:53709813 | G | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+4571C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709813 | |||||||
| chr2:53709823 | T | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.980+4561A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709823 | |||||||
| chr2:53709828 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.980+4556C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709828 | |||||||
| chr2:53709907 | G | C | 1 | a0005c0006t0002g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.980+4477C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709907 | |||||||
| chr2:53710040 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(200): Show |
205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.980+4344G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710040 | |||||||
| chr2:53710100 | A | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.980+4284T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710100 | |||||||
| chr2:53710279 | A | G | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+4105T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710279 | |||||||
| chr2:53710330 | T | C | 1 | a0001c0001t0004g0080 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.980+4054A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710330 | |||||||
| chr2:53710333 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+4051A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710333 | |||||||
| chr2:53710365 | A | T | 213 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.980+4019T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710365 | |||||||
| chr2:53710378 | T | A | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.980+4006A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710378 | |||||||
| chr2:53710467 | G | C | 1 | a0001c0003t0007g0284 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.980+3917C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710467 | |||||||
| chr2:53710601 | T | G | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.980+3783A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710601 | |||||||
| chr2:53710803 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.980+3581T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710803 | |||||||
| chr2:53710816 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+3568A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710816 | |||||||
| chr2:53710864 | C | T | 1 | a0001c0002t0002g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.980+3520G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710864 | |||||||
| chr2:53710897 | C | A | 1 | a0001c0001t0003g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.980+3487G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710897 | |||||||
| chr2:53710901 | G | C | 218 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
221 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.980+3483C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710901 | |||||||
| chr2:53710970 | CA | C | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(199): Show |
204 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.980+3413delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710970 | |||||||
| chr2:53711027 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+3357C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711027 | |||||||
| chr2:53711082 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.980+3302C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711082 | |||||||
| chr2:53711286 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+3098A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711286 | |||||||
| chr2:53711355 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.980+3029A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711355 | |||||||
| chr2:53711557 | T | C | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.980+2827A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711557 | |||||||
| chr2:53711635 | A | G | 2 | a0001c0003t0007g0283 a0001c0003t0007g0284 |
2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.980+2749T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711635 | |||||||
| chr2:53711639 | T | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0126 |
3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.980+2745A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711639 | |||||||
| chr2:53711761 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980+2623C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711761 | |||||||
| chr2:53711908 | C | T | 53 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0111 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.980+2476G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711908 | |||||||
| chr2:53711949 | T | C | 10 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(7): Show |
10 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.980+2435A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711949 | |||||||
| chr2:53712001 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0079 others(1): Show |
4 | HG02129.hp1 NA18943.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+2383G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712001 | |||||||
| chr2:53712057 | T | G | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.980+2327A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712057 | |||||||
| chr2:53712147 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.980+2237A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712147 | |||||||
| chr2:53712216 | C | CA | 11 | a0001c0001t0001g0129 a0001c0001t0001g0150 a0001c0001t0001g0210 others(8): Show |
11 | HG02572.hp2 HG02818.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+2167dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712216 | |||||||
| chr2:53712216 | CA | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(27): Show |
31 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.980+2167delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712216 | |||||||
| chr2:53712242 | G | T | 3 | a0001c0003t0002g0285 a0001c0003t0002g0287 a0001c0003t0002g0288 |
3 | HG02155.hp1 NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.980+2142C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712242 | |||||||
| chr2:53712290 | T | C | 52 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.980+2094A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712290 | |||||||
| chr2:53712411 | C | T | 227 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
230 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.980+1973G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712411 | |||||||
| chr2:53712539 | G | A | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+1845C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712539 | |||||||
| chr2:53712602 | CA | C | 4 | a0001c0002t0002g0219 a0001c0002t0002g0224 a0001c0002t0002g0225 others(1): Show |
4 | HG00423.hp1 HG02074.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1781delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712602 | |||||||
| chr2:53712635 | T | C | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980+1749A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712635 | |||||||
| chr2:53712745 | A | AAC | 21 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0053 others(18): Show |
21 | HG00438.hp2 HG01074.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.980+1637_980+1638d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712745 | |||||||
| chr2:53712745 | AAC | A | 114 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(111): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.980+1637_980+1638d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712745 | |||||||
| chr2:53712767 | C | T | 1 | a0001c0001t0004g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.980+1617G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712767 | |||||||
| chr2:53712769 | G | GGC | 10 | a0001c0001t0001g0112 a0001c0001t0001g0310 a0001c0001t0002g0227 others(7): Show |
10 | HG01255.hp1 HG02280.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.980+1613_980+1614d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712769 | |||||||
| chr2:53712772 | G | A | 2 | a0001c0003t0002g0301 a0001c0003t0002g0302 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.980+1612C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712772 | |||||||
| chr2:53712774 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.980+1610C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712774 | |||||||
| chr2:53712778 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.980+1606C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712778 | |||||||
| chr2:53712780 | G | A | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+1604C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712780 | |||||||
| chr2:53712822 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.980+1562C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712822 | |||||||
| chr2:53712825 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1559G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712825 | |||||||
| chr2:53712946 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980+1438C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712946 | |||||||
| chr2:53713109 | G | A | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+1275C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713109 | |||||||
| chr2:53713333 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980+1051A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713333 | |||||||
| chr2:53713383 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1001A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713383 | |||||||
| chr2:53713586 | G | T | 215 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.980+798C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713586 | |||||||
| chr2:53713651 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.980+733C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713651 | |||||||
| chr2:53713925 | T | A | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.980+459A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713925 | |||||||
| chr2:53713988 | A | T | 123 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.980+396T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713988 | |||||||
| chr2:53714052 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.980+332A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714052 | |||||||
| chr2:53714086 | T | C | 1 | a0001c0003t0014g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.980+298A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714086 | |||||||
| chr2:53714103 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.980+281G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714103 | |||||||
| chr2:53714131 | T | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.980+253A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714131 | |||||||
| chr2:53714143 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+241T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714143 | |||||||
| chr2:53714186 | G | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+198C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714186 | |||||||
| chr2:53714218 | G | A | 1 | a0001c0001t0008g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.980+166C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714218 | |||||||
| chr2:53714276 | T | A | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+108A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714276 | |||||||
| chr2:53714305 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0003g0145 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+79G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714305 | |||||||
| chr2:53714375 | T | C | 7 | a0001c0001t0009g0178 a0001c0001t0009g0191 a0001c0001t0009g0198 others(4): Show |
7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+9A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714375 | |||||||
| chr2:53714607 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.783-26A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714607 | |||||||
| chr2:53714622 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0003g0145 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.783-41A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714622 | |||||||
| chr2:53714806 | T | C | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.783-225A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714806 | |||||||
| chr2:53715001 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.783-420G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715001 | |||||||
| chr2:53715204 | A | G | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.783-623T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715204 | |||||||
| chr2:53715216 | C | A | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.783-635G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715216 | |||||||
| chr2:53715230 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.783-649T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715230 | |||||||
| chr2:53715242 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0004g0161 |
3 | NA18951.hp1 NA18973.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.783-661T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715242 | |||||||
| chr2:53715312 | G | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0211 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-731C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715312 | |||||||
| chr2:53715346 | C | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0211 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-765G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715346 | |||||||
| chr2:53715441 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0004g0120 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.783-860G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715441 | |||||||
| chr2:53715452 | G | C | 14 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(11): Show |
14 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.783-871C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715452 | |||||||
| chr2:53715564 | A | G | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.783-983T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715564 | |||||||
| chr2:53715662 | C | G | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.782+904G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715662 | |||||||
| chr2:53715672 | T | C | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.782+894A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715672 | |||||||
| chr2:53715788 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.782+778G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715788 | |||||||
| chr2:53715843 | T | C | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.782+723A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715843 | |||||||
| chr2:53715947 | T | TATTGACT others(48): Show |
1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.782+564_782+618dup others(55): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715947 | |||||||
| chr2:53716002 | C | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
148 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.782+564G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716002 | |||||||
| chr2:53716024 | G | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.782+542C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716024 | |||||||
| chr2:53716202 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.782+364C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716202 | |||||||
| chr2:53716249 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.782+317C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716249 | |||||||
| chr2:53716251 | C | A | 1 | a0001c0002t0002g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.782+315G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716251 | |||||||
| chr2:53716404 | G | C | 1 | a0001c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.782+162C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716404 | |||||||
| chr2:53716559 | C | T | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.782+7G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716559 | |||||||
| chr2:53716813 | G | C | 3 | a0001c0003t0005g0328 a0001c0003t0005g0331 a0001c0003t0005g0332 |
3 | HG00733.hp1 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.605-70C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716813 | |||||||
| chr2:53716833 | C | G | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.605-90G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716833 | |||||||
| chr2:53716995 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.605-252A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716995 | |||||||
| chr2:53717105 | A | C | 40 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0111 others(37): Show |
40 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.605-362T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717105 | |||||||
| chr2:53717205 | T | A | 52 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.605-462A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717205 | |||||||
| chr2:53717226 | G | A | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(98): Show |
101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.605-483C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717226 | |||||||
| chr2:53717229 | A | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0211 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-486T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717229 | |||||||
| chr2:53717229 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0035 others(95): Show |
100 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.605-486T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717229 | |||||||
| chr2:53717290 | C | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
99 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.605-547G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717290 | |||||||
| chr2:53717323 | T | G | 1 | a0001c0002t0007g0241 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.605-580A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717323 | |||||||
| chr2:53717355 | G | A | 1 | a0001c0003t0005g0332 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.605-612C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717355 | |||||||
| chr2:53717606 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.605-863G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717606 | |||||||
| chr2:53717659 | A | T | 1 | a0001c0001t0003g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.605-916T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717659 | |||||||
| chr2:53717676 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(104): Show |
107 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.605-933C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717676 | |||||||
| chr2:53718175 | G | A | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(98): Show |
101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.605-1432C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718175 | |||||||
| chr2:53718203 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(88): Show |
93 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.605-1460C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718203 | |||||||
| chr2:53718279 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(89): Show |
94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1536C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718279 | |||||||
| chr2:53718284 | A | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(89): Show |
94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1541T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718284 | |||||||
| chr2:53718286 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.605-1543C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718286 | |||||||
| chr2:53718286 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(89): Show |
94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1543C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718286 | |||||||
| chr2:53718287 | T | TA | 92 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(89): Show |
94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1545_605-1544i others(3): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718287 | |||||||
| chr2:53718297 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(97): Show |
102 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.605-1554A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718297 | |||||||
| chr2:53718348 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0004g0120 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.605-1605A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718348 | |||||||
| chr2:53718451 | A | G | 1 | a0001c0002t0002g0262 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.605-1708T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718451 | |||||||
| chr2:53718574 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.605-1831T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718574 | |||||||
| chr2:53718661 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.605-1918A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718661 | |||||||
| chr2:53718742 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.605-1999C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718742 | |||||||
| chr2:53718773 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-2030T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718773 | |||||||
| chr2:53718984 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.605-2241C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718984 | |||||||
| chr2:53719151 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0056 |
2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.605-2408A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719151 | |||||||
| chr2:53719175 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.605-2432C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719175 | |||||||
| chr2:53719280 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.605-2537C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719280 | |||||||
| chr2:53719294 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0060 a0001c0001t0001g0067 others(2): Show |
6 | HG00558.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.605-2551C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719294 | |||||||
| chr2:53719502 | A | T | 16 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-2759T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719502 | |||||||
| chr2:53719648 | C | G | 9 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-2905G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719648 | |||||||
| chr2:53719685 | A | T | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.605-2942T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719685 | |||||||
| chr2:53719706 | G | T | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.605-2963C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719706 | |||||||
| chr2:53719963 | C | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.605-3220G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719963 | |||||||
| chr2:53720046 | G | A | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.605-3303C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720046 | |||||||
| chr2:53720138 | C | CA | 8 | a0001c0001t0001g0093 a0001c0001t0001g0148 a0001c0001t0001g0165 others(5): Show |
8 | HG01891.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-3396dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | |||||||
| chr2:53720138 | CA | C | 170 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(167): Show |
171 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.605-3396delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | |||||||
| chr2:53720138 | CAA | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-3397_605-3396d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | |||||||
| chr2:53720278 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
218 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.605-3535G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720278 | |||||||
| chr2:53720397 | T | A | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.605-3654A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720397 | |||||||
| chr2:53720580 | G | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(54): Show |
57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.605-3837C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720580 | |||||||
| chr2:53720707 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-3964C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720707 | |||||||
| chr2:53720820 | C | A | 1 | a0006c0010t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.605-4077G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720820 | |||||||
| chr2:53720899 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0341 |
2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.605-4156A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720899 | |||||||
| chr2:53720963 | A | G | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.605-4220T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720963 | |||||||
| chr2:53720989 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0003g0117 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.605-4246G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720989 | |||||||
| chr2:53720991 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.605-4248G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720991 | |||||||
| chr2:53721123 | T | TATAA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(112): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.605-4384_605-4381d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | |||||||
| chr2:53721123 | T | TATAAATA others(1): Show |
11 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0072 others(8): Show |
12 | HG00558.hp1 HG01257.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.605-4388_605-4381d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | |||||||
| chr2:53721123 | TATAA | T | 14 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0209 others(11): Show |
14 | HG00408.hp2 HG01069.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.605-4384_605-4381d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | |||||||
| chr2:53721123 | TATAAATA others(1): Show |
T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0119 others(5): Show |
8 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-4388_605-4381d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | |||||||
| chr2:53721123 | TATAAATA others(5): Show |
T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0003t0002g0295 |
3 | HG01070.hp2 HG01071.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.605-4392_605-4381d others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | |||||||
| chr2:53721285 | T | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-4542A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721285 | |||||||
| chr2:53721344 | C | G | 1 | a0001c0003t0002g0287 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.605-4601G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721344 | |||||||
| chr2:53721352 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0081 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-4609G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721352 | |||||||
| chr2:53721398 | C | CA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0324 a0001c0001t0003g0171 others(12): Show |
15 | HG01515.hp2 HG02145.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.605-4656dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | |||||||
| chr2:53721398 | C | CAA | 16 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0316 others(13): Show |
16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-4657_605-4656d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | |||||||
| chr2:53721398 | CA | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(138): Show |
143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.605-4656delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | |||||||
| chr2:53721430 | A | ACATAGTG others(1): Show |
20 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0019 others(17): Show |
20 | HG00673.hp1 HG00673.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.605-4695_605-4688d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721430 | |||||||
| chr2:53721512 | G | A | 53 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0111 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.605-4769C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721512 | |||||||
| chr2:53721799 | C | A | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.605-5056G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721799 | |||||||
| chr2:53721854 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-5111A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721854 | |||||||
| chr2:53721854 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0004g0113 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.605-5111A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721854 | |||||||
| chr2:53721936 | C | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(283): Show |
290 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.605-5193G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721936 | |||||||
| chr2:53721965 | G | A | 1 | a0001c0001t0004g0025 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.605-5222C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721965 | |||||||
| chr2:53721987 | T | C | 14 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(11): Show |
14 | HG01167.hp1 HG02615.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.605-5244A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721987 | |||||||
| chr2:53722086 | G | C | 1 | a0006c0010t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.605-5343C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722086 | |||||||
| chr2:53722100 | A | G | 13 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(10): Show |
13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.605-5357T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722100 | |||||||
| chr2:53722156 | T | C | 9 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-5413A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722156 | |||||||
| chr2:53722173 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-5430A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722173 | |||||||
| chr2:53722179 | A | T | 8 | a0001c0001t0003g0217 a0001c0001t0008g0028 a0001c0001t0008g0030 others(5): Show |
8 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-5436T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722179 | |||||||
| chr2:53722193 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.605-5450A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722193 | |||||||
| chr2:53722348 | C | G | 1 | a0001c0001t0003g0184 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.605-5605G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722348 | |||||||
| chr2:53722404 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.605-5661C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722404 | |||||||
| chr2:53722413 | T | C | 9 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-5670A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722413 | |||||||
| chr2:53722496 | T | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(15): Show |
18 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.605-5753A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722496 | |||||||
| chr2:53722538 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.605-5795A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722538 | |||||||
| chr2:53722679 | T | C | 3 | a0001c0001t0011g0095 a0001c0003t0002g0292 a0001c0003t0003g0308 |
3 | HG00323.hp1 HG02074.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.605-5936A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722679 | |||||||
| chr2:53722808 | C | T | 53 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0111 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.604+5904G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722808 | |||||||
| chr2:53722985 | A | C | 1 | a0001c0003t0002g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.604+5727T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722985 | |||||||
| chr2:53723165 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0140 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+5547G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723165 | |||||||
| chr2:53723189 | T | C | 1 | a0001c0001t0003g0196 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.604+5523A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723189 | |||||||
| chr2:53723234 | A | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+5478T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723234 | |||||||
| chr2:53723248 | A | T | 22 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(19): Show |
22 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.604+5464T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723248 | |||||||
| chr2:53723394 | C | T | 1 | a0001c0001t0004g0025 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.604+5318G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723394 | |||||||
| chr2:53723397 | T | C | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604+5315A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723397 | |||||||
| chr2:53723544 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+5168T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723544 | |||||||
| chr2:53723569 | A | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+5143T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723569 | |||||||
| chr2:53723615 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0004g0120 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.604+5097G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723615 | |||||||
| chr2:53723647 | T | A | 3 | a0001c0003t0002g0295 a0001c0003t0002g0296 a0001c0003t0002g0297 |
3 | HG03041.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.604+5065A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723647 | |||||||
| chr2:53723737 | C | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0209 a0001c0003t0002g0280 |
3 | HG01891.hp2 NA18943.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.604+4975G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723737 | |||||||
| chr2:53723875 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+4837T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723875 | |||||||
| chr2:53724171 | G | A | 2 | a0001c0003t0001g0304 a0001c0003t0001g0305 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.604+4541C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724171 | |||||||
| chr2:53724199 | T | C | 51 | a0001c0001t0003g0217 a0001c0001t0003g0340 a0001c0003t0001g0304 others(48): Show |
51 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.604+4513A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724199 | |||||||
| chr2:53724252 | A | G | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.604+4460T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724252 | |||||||
| chr2:53724317 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.604+4395C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724317 | |||||||
| chr2:53724395 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.604+4317T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724395 | |||||||
| chr2:53724418 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.604+4294C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724418 | |||||||
| chr2:53724460 | A | C | 4 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.604+4252T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724460 | |||||||
| chr2:53724565 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0002g0130 |
3 | HG00558.hp1 NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.604+4147G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724565 | |||||||
| chr2:53724736 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.604+3976T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724736 | |||||||
| chr2:53724897 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.604+3815T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724897 | |||||||
| chr2:53724902 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0004g0013 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.604+3810G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724902 | |||||||
| chr2:53724981 | A | G | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+3731T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724981 | |||||||
| chr2:53725041 | A | G | 83 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.604+3671T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725041 | |||||||
| chr2:53725256 | T | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0126 |
3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.604+3456A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725256 | |||||||
| chr2:53725377 | C | T | 1 | a0001c0001t0003g0184 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.604+3335G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725377 | |||||||
| chr2:53725428 | G | A | 46 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(43): Show |
48 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.604+3284C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725428 | |||||||
| chr2:53725453 | TA | T | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.604+3258delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725453 | |||||||
| chr2:53725496 | C | T | 1 | a0001c0002t0002g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.604+3216G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725496 | |||||||
| chr2:53725662 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+3050C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725662 | |||||||
| chr2:53725683 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604+3029G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725683 | |||||||
| chr2:53725796 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.604+2916A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725796 | |||||||
| chr2:53725871 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+2841A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725871 | |||||||
| chr2:53726026 | G | T | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.604+2686C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726026 | |||||||
| chr2:53726231 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0003g0117 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.604+2481C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726231 | |||||||
| chr2:53726251 | A | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2461T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726251 | |||||||
| chr2:53726257 | A | AT | 85 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0055 others(82): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.604+2454dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | |||||||
| chr2:53726257 | A | ATT | 11 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(8): Show |
11 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.604+2453_604+2454d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | |||||||
| chr2:53726257 | AT | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0100 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.604+2454delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | |||||||
| chr2:53726314 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0133 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.604+2398C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726314 | |||||||
| chr2:53726322 | G | A | 2 | a0001c0003t0002g0278 a0001c0003t0002g0299 |
2 | NA19002.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.604+2390C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726322 | |||||||
| chr2:53726519 | C | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2193G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726519 | |||||||
| chr2:53726597 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.604+2115A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726597 | |||||||
| chr2:53726631 | T | C | 1 | a0001c0003t0003g0308 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.604+2081A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726631 | |||||||
| chr2:53726687 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0096 a0001c0001t0005g0003 |
4 | HG01516.hp1 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+2025A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726687 | |||||||
| chr2:53726692 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+2020T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726692 | |||||||
| chr2:53726720 | G | A | 1 | a0001c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.604+1992C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726720 | |||||||
| chr2:53726759 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.604+1953G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726759 | |||||||
| chr2:53726809 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.604+1903C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726809 | |||||||
| chr2:53726830 | C | G | 216 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.604+1882G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726830 | |||||||
| chr2:53726903 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+1809C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726903 | |||||||
| chr2:53726986 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(27): Show |
31 | HG00099.hp1 HG00408.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.604+1726T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726986 | |||||||
| chr2:53727113 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.604+1599A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727113 | |||||||
| chr2:53727125 | A | C | 1 | a0001c0001t0008g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604+1587T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727125 | |||||||
| chr2:53727131 | C | T | 2 | a0001c0003t0002g0290 a0001c0003t0006g0300 |
2 | HG01175.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.604+1581G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727131 | |||||||
| chr2:53727215 | G | C | 7 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0019 others(4): Show |
7 | HG00673.hp2 HG02056.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.604+1497C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727215 | |||||||
| chr2:53727466 | TA | T | 57 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0255 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+1245delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727466 | |||||||
| chr2:53727528 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604+1184A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727528 | |||||||
| chr2:53727544 | C | G | 177 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0140 others(174): Show |
179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.604+1168G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727544 | |||||||
| chr2:53727563 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.604+1149C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727563 | |||||||
| chr2:53727676 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.604+1036A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727676 | |||||||
| chr2:53727705 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+1007T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727705 | |||||||
| chr2:53727752 | G | C | 2 | a0001c0002t0002g0220 a0001c0002t0002g0244 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.604+960C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727752 | |||||||
| chr2:53727757 | C | G | 1 | a0001c0001t0008g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.604+955G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727757 | |||||||
| chr2:53727806 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+906T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727806 | |||||||
| chr2:53728051 | T | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+661A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728051 | |||||||
| chr2:53728052 | A | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.604+660T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728052 | |||||||
| chr2:53728157 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.604+555C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728157 | |||||||
| chr2:53728206 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604+506A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728206 | |||||||
| chr2:53728334 | C | T | 37 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(34): Show |
37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.604+378G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728334 | |||||||
| chr2:53728341 | G | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.604+371C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728341 | |||||||
| chr2:53728352 | A | C | 196 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.604+360T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728352 | |||||||
| chr2:53728376 | A | C | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(114): Show |
117 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.604+336T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728376 | |||||||
| chr2:53728460 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0160 a0001c0001t0001g0164 others(2): Show |
6 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+252C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728460 | |||||||
| chr2:53728524 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.604+188G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728524 | |||||||
| chr2:53728604 | C | T | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+108G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728604 | |||||||
| chr2:53728684 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.604+28G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728684 | |||||||
| chr2:53729156 | A | G | 1 | a0001c0001t0015g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.468+302T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729156 | |||||||
| chr2:53729234 | T | C | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+224A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729234 | |||||||
| chr2:53729239 | T | C | 2 | a0001c0001t0003g0179 a0001c0001t0003g0182 |
2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.468+219A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729239 | |||||||
| chr2:53729701 | A | G | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.356-131T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729701 | |||||||
| chr2:53729710 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.356-140A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729710 | |||||||
| chr2:53729721 | C | A | 1 | a0001c0002t0002g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.356-151G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729721 | |||||||
| chr2:53729746 | T | G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(52): Show |
55 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.356-176A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729746 | |||||||
| chr2:53729779 | T | TAAAAGAC others(318): Show |
1 | a0001c0001t0001g0037 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.356-210_356-209ins others(325): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729779 | |||||||
| chr2:53729843 | C | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-273G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729843 | |||||||
| chr2:53729902 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-332G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729902 | |||||||
| chr2:53729947 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0059 others(1): Show |
5 | NA18983.hp1 NA19004.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-377G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729947 | |||||||
| chr2:53729961 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-391C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729961 | |||||||
| chr2:53729983 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0078 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.356-413A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729983 | |||||||
| chr2:53730039 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-469A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730039 | |||||||
| chr2:53730135 | T | C | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.356-565A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730135 | |||||||
| chr2:53730203 | T | C | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-633A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730203 | |||||||
| chr2:53730224 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.356-654T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730224 | |||||||
| chr2:53730238 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0211 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.356-668A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730238 | |||||||
| chr2:53730329 | C | T | 2 | a0001c0003t0007g0283 a0001c0003t0007g0284 |
2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.356-759G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730329 | |||||||
| chr2:53730553 | G | A | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.356-983C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730553 | |||||||
| chr2:53730645 | A | C | 1 | a0001c0002t0002g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.356-1075T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730645 | |||||||
| chr2:53730665 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.356-1095C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730665 | |||||||
| chr2:53730682 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02080.hp1 NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.356-1112A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730682 | |||||||
| chr2:53730837 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.356-1267C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730837 | |||||||
| chr2:53730935 | A | C | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-1365T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730935 | |||||||
| chr2:53730999 | C | T | 193 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
196 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.356-1429G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730999 | |||||||
| chr2:53731079 | C | T | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-1509G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731079 | |||||||
| chr2:53731121 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1551T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731121 | |||||||
| chr2:53731172 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.356-1602G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731172 | |||||||
| chr2:53731183 | C | T | 3 | a0001c0003t0005g0311 a0001c0003t0011g0329 a0007c0007t0005g0342 |
3 | HG01168.hp1 HG01256.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.356-1613G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731183 | |||||||
| chr2:53731271 | A | G | 60 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(57): Show |
60 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.356-1701T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731271 | |||||||
| chr2:53731272 | C | T | 37 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(34): Show |
37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-1702G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731272 | |||||||
| chr2:53731345 | T | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1775A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731345 | |||||||
| chr2:53731408 | A | AAAAAC | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1843_356-1839d others(7): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731408 | |||||||
| chr2:53731497 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.356-1927C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731497 | |||||||
| chr2:53731542 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-1972A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731542 | |||||||
| chr2:53731692 | G | A | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.356-2122C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731692 | |||||||
| chr2:53731713 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-2143G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731713 | |||||||
| chr2:53731724 | C | T | 195 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(192): Show |
198 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.356-2154G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731724 | |||||||
| chr2:53731753 | A | C | 1 | a0001c0003t0002g0290 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.356-2183T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731753 | |||||||
| chr2:53731782 | C | A | 116 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.356-2212G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731782 | |||||||
| chr2:53731801 | C | T | 1 | a0001c0003t0002g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.356-2231G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731801 | |||||||
| chr2:53731816 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.356-2246G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731816 | |||||||
| chr2:53731845 | G | A | 1 | a0001c0002t0002g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.356-2275C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731845 | |||||||
| chr2:53731905 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.356-2335C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731905 | |||||||
| chr2:53732027 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.356-2457C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732027 | |||||||
| chr2:53732061 | C | T | 37 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(34): Show |
37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-2491G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732061 | |||||||
| chr2:53732084 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.356-2514C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732084 | |||||||
| chr2:53732207 | C | T | 9 | a0001c0001t0001g0164 a0001c0002t0002g0219 a0001c0002t0002g0222 others(6): Show |
9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-2637G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732207 | |||||||
| chr2:53732432 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
93 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.356-2862G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732432 | |||||||
| chr2:53732500 | T | C | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-2930A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732500 | |||||||
| chr2:53732525 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.356-2955A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732525 | |||||||
| chr2:53732759 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-3189G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732759 | |||||||
| chr2:53732827 | G | C | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-3257C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732827 | |||||||
| chr2:53732956 | G | C | 12 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.356-3386C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732956 | |||||||
| chr2:53733092 | C | T | 1 | a0006c0010t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.356-3522G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733092 | |||||||
| chr2:53733297 | G | C | 1 | a0001c0001t0012g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.356-3727C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733297 | |||||||
| chr2:53733445 | CT | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
151 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.356-3876delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733445 | |||||||
| chr2:53733491 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.356-3921C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733491 | |||||||
| chr2:53733615 | T | C | 2 | a0001c0002t0002g0263 a0001c0002t0002g0264 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.356-4045A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733615 | |||||||
| chr2:53733716 | C | T | 11 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(8): Show |
11 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4146G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733716 | |||||||
| chr2:53733810 | G | A | 54 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(51): Show |
56 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-4240C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733810 | |||||||
| chr2:53733835 | A | G | 220 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.356-4265T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733835 | |||||||
| chr2:53733915 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-4345G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733915 | |||||||
| chr2:53733990 | G | C | 1 | a0001c0001t0001g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.356-4420C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733990 | |||||||
| chr2:53734071 | G | A | 2 | a0001c0003t0002g0287 a0001c0003t0002g0288 |
2 | NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.356-4501C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734071 | |||||||
| chr2:53734118 | C | G | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-4548G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734118 | |||||||
| chr2:53734275 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-4705G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734275 | |||||||
| chr2:53734438 | T | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.356-4868A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734438 | |||||||
| chr2:53734613 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.356-5043A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734613 | |||||||
| chr2:53734717 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.356-5147G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734717 | |||||||
| chr2:53734723 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-5153C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734723 | |||||||
| chr2:53734874 | G | C | 1 | a0001c0002t0006g0270 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.356-5304C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734874 | |||||||
| chr2:53734891 | A | AT | 6 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-5322dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734891 | |||||||
| chr2:53734918 | G | GT | 62 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0096 others(59): Show |
62 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.356-5349dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734918 | |||||||
| chr2:53734918 | GT | G | 129 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(126): Show |
131 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.356-5349delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734918 | |||||||
| chr2:53735016 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.356-5446A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735016 | |||||||
| chr2:53735172 | G | A | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(53): Show |
56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.356-5602C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735172 | |||||||
| chr2:53735212 | G | A | 52 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.356-5642C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735212 | |||||||
| chr2:53735215 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.356-5645G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735215 | |||||||
| chr2:53735345 | T | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-5775A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735345 | |||||||
| chr2:53735485 | T | TA | 169 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
170 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.356-5916dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735485 | |||||||
| chr2:53735485 | T | TAA | 7 | a0001c0001t0003g0217 a0001c0002t0002g0259 a0001c0002t0002g0266 others(4): Show |
7 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-5917_356-5916d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735485 | |||||||
| chr2:53735519 | CATAGAT | C | 5 | a0001c0002t0002g0229 a0001c0002t0002g0250 a0001c0002t0002g0251 others(2): Show |
5 | NA18941.hp2 NA18961.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-5955_356-5950d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735519 | |||||||
| chr2:53735591 | C | T | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.356-6021G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735591 | |||||||
| chr2:53735642 | A | C | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.356-6072T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735642 | |||||||
| chr2:53735699 | A | C | 221 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(218): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.356-6129T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735699 | |||||||
| chr2:53735792 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-6222A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735792 | |||||||
| chr2:53735911 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356-6341T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735911 | |||||||
| chr2:53735998 | T | TA | 71 | a0001c0001t0001g0110 a0001c0001t0001g0148 a0001c0001t0001g0150 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.356-6429dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735998 | |||||||
| chr2:53735998 | TA | T | 15 | a0001c0001t0001g0037 a0001c0001t0001g0058 a0001c0001t0001g0063 others(12): Show |
15 | HG00733.hp1 HG01069.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.356-6429delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735998 | |||||||
| chr2:53736105 | A | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(53): Show |
56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.356-6535T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736105 | |||||||
| chr2:53736179 | T | C | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.356-6609A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736179 | |||||||
| chr2:53736450 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.356-6880C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736450 | |||||||
| chr2:53736479 | G | A | 203 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
206 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.356-6909C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736479 | |||||||
| chr2:53736561 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.356-6991A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736561 | |||||||
| chr2:53736567 | C | T | 1 | a0001c0003t0002g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.356-6997G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736567 | |||||||
| chr2:53736700 | G | GA | 52 | a0001c0001t0001g0129 a0001c0001t0002g0227 a0001c0001t0002g0228 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.356-7131dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | |||||||
| chr2:53736700 | GA | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
85 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.356-7131delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | |||||||
| chr2:53736700 | GAA | G | 55 | a0001c0001t0003g0340 a0001c0001t0008g0208 a0001c0003t0001g0304 others(52): Show |
55 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.356-7132_356-7131d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | |||||||
| chr2:53736874 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0004g0149 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.356-7304G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736874 | |||||||
| chr2:53737028 | T | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-7458A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737028 | |||||||
| chr2:53737031 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-7461T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737031 | |||||||
| chr2:53737150 | T | C | 224 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.356-7580A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737150 | |||||||
| chr2:53737222 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-7652G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737222 | |||||||
| chr2:53737369 | A | G | 62 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(59): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.356-7799T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737369 | |||||||
| chr2:53737429 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.356-7859T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737429 | |||||||
| chr2:53737502 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-7932C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737502 | |||||||
| chr2:53737509 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0003g0171 others(2): Show |
5 | HG00621.hp1 HG02080.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-7939T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737509 | |||||||
| chr2:53737582 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-8012G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737582 | |||||||
| chr2:53737601 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356-8031G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737601 | |||||||
| chr2:53737724 | G | GA | 20 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0110 others(17): Show |
20 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.356-8155dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737724 | |||||||
| chr2:53737724 | GA | G | 19 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0101 others(16): Show |
19 | HG00408.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.356-8155delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737724 | |||||||
| chr2:53737787 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0169 a0001c0001t0003g0189 |
4 | NA18944.hp2 NA18950.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-8217C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737787 | |||||||
| chr2:53738026 | T | C | 7 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0019 others(4): Show |
7 | HG00673.hp2 HG02056.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.356-8456A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738026 | |||||||
| chr2:53738124 | G | T | 2 | a0003c0005t0005g0336 a0003c0005t0005g0337 |
2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.356-8554C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738124 | |||||||
| chr2:53738131 | A | C | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.356-8561T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738131 | |||||||
| chr2:53738205 | T | C | 7 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0004g0271 others(4): Show |
7 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-8635A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738205 | |||||||
| chr2:53738252 | G | A | 213 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.356-8682C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738252 | |||||||
| chr2:53738274 | T | G | 2 | a0001c0001t0002g0153 a0002c0004t0013g0011 |
2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.356-8704A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738274 | |||||||
| chr2:53738387 | C | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-8817G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738387 | |||||||
| chr2:53738430 | T | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-8860A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738430 | |||||||
| chr2:53738470 | G | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-8900C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738470 | |||||||
| chr2:53738532 | A | G | 1 | a0001c0003t0002g0289 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.356-8962T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738532 | |||||||
| chr2:53738551 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-8981A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738551 | |||||||
| chr2:53738640 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356-9070A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738640 | |||||||
| chr2:53738684 | G | A | 50 | a0001c0001t0003g0340 a0001c0003t0001g0304 a0001c0003t0001g0305 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.356-9114C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738684 | |||||||
| chr2:53738720 | G | C | 1 | a0001c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.356-9150C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738720 | |||||||
| chr2:53738913 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-9343A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738913 | |||||||
| chr2:53739002 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356-9432G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739002 | |||||||
| chr2:53739084 | T | C | 1 | a0001c0003t0002g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.356-9514A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739084 | |||||||
| chr2:53739111 | G | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-9541C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739111 | |||||||
| chr2:53739126 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.356-9556C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739126 | |||||||
| chr2:53739364 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.356-9794C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739364 | |||||||
| chr2:53739712 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-10142C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739712 | |||||||
| chr2:53739955 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.356-10385A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739955 | |||||||
| chr2:53740034 | A | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.356-10464T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740034 | |||||||
| chr2:53740109 | A | G | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.356-10539T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740109 | |||||||
| chr2:53740132 | C | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0004g0125 |
3 | NA18965.hp1 NA18967.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.356-10562G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740132 | |||||||
| chr2:53740194 | G | C | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355+10589C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740194 | |||||||
| chr2:53740200 | C | T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0341 |
2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.355+10583G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740200 | |||||||
| chr2:53740224 | C | T | 1 | a0001c0002t0002g0232 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.355+10559G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740224 | |||||||
| chr2:53740349 | G | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0006g0142 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.355+10434C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740349 | |||||||
| chr2:53740443 | T | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0126 |
3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.355+10340A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740443 | |||||||
| chr2:53740559 | T | A | 46 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(43): Show |
46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.355+10224A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740559 | |||||||
| chr2:53740646 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355+10137A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740646 | |||||||
| chr2:53740693 | T | C | 14 | a0001c0001t0003g0217 a0001c0001t0003g0340 a0001c0003t0005g0311 others(11): Show |
14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+10090A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740693 | |||||||
| chr2:53740870 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+9913T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740870 | |||||||
| chr2:53740968 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+9815G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740968 | |||||||
| chr2:53740979 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.355+9804T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740979 | |||||||
| chr2:53741021 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0152 |
2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.355+9762A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741021 | |||||||
| chr2:53741097 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.355+9686G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741097 | |||||||
| chr2:53741637 | C | T | 204 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.355+9146G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741637 | |||||||
| chr2:53741828 | A | G | 11 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0049 others(8): Show |
11 | HG00438.hp2 HG02027.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+8955T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741828 | |||||||
| chr2:53742107 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.355+8676A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742107 | |||||||
| chr2:53742432 | C | T | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+8351G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742432 | |||||||
| chr2:53742461 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.355+8322A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742461 | |||||||
| chr2:53742734 | TA | T | 204 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.355+8048delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742734 | |||||||
| chr2:53742789 | A | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+7994T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742789 | |||||||
| chr2:53742880 | A | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+7903T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742880 | |||||||
| chr2:53743102 | C | A | 14 | a0001c0001t0003g0217 a0001c0001t0003g0340 a0001c0003t0005g0311 others(11): Show |
14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+7681G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743102 | |||||||
| chr2:53743127 | G | T | 54 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0255 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.355+7656C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743127 | |||||||
| chr2:53743164 | C | CT | 13 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0064 others(10): Show |
13 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+7618dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743164 | |||||||
| chr2:53743164 | CT | C | 160 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
164 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.355+7618delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743164 | |||||||
| chr2:53743209 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0004g0013 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.355+7574A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743209 | |||||||
| chr2:53743800 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+6983G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743800 | |||||||
| chr2:53743874 | C | T | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+6909G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743874 | |||||||
| chr2:53743882 | A | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+6901T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743882 | |||||||
| chr2:53743949 | A | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0107 others(1): Show |
5 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+6834T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743949 | |||||||
| chr2:53743957 | C | T | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6826G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743957 | |||||||
| chr2:53744042 | C | CA | 56 | a0001c0001t0001g0056 a0001c0001t0001g0121 a0001c0001t0001g0148 others(53): Show |
56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.355+6740dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744042 | |||||||
| chr2:53744099 | G | A | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355+6684C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744099 | |||||||
| chr2:53744114 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.355+6669G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744114 | |||||||
| chr2:53744129 | C | G | 1 | a0001c0001t0004g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.355+6654G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744129 | |||||||
| chr2:53744195 | T | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+6588A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744195 | |||||||
| chr2:53744220 | C | CA | 6 | a0001c0001t0001g0110 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG02080.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+6562dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744220 | |||||||
| chr2:53744245 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+6538C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744245 | |||||||
| chr2:53744265 | T | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+6518A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744265 | |||||||
| chr2:53744363 | AG | A | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6419delC | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744363 | |||||||
| chr2:53744372 | G | A | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6411C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744372 | |||||||
| chr2:53744379 | T | C | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6404A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744379 | |||||||
| chr2:53744384 | C | CAAAA | 32 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(29): Show |
32 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.355+6395_355+6398d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | |||||||
| chr2:53744384 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(15): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | |||||||
| chr2:53744384 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0145 a0001c0001t0003g0146 a0001c0001t0003g0147 others(1): Show |
4 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+6398_355+6399i others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | |||||||
| chr2:53744384 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(17): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | |||||||
| chr2:53744384 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(18): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | |||||||
| chr2:53744392 | T | A | 44 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(41): Show |
44 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.355+6391A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744392 | |||||||
| chr2:53744396 | T | A | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6387A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744396 | |||||||
| chr2:53744400 | A | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0066 |
2 | NA18952.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.355+6383T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744400 | |||||||
| chr2:53744406 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(15): Show |
18 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.355+6377T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744406 | |||||||
| chr2:53744503 | T | C | 13 | a0001c0001t0003g0340 a0001c0003t0005g0311 a0001c0003t0005g0328 others(10): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+6280A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744503 | |||||||
| chr2:53744534 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+6249A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744534 | |||||||
| chr2:53744681 | G | A | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.355+6102C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744681 | |||||||
| chr2:53745008 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.355+5775G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745008 | |||||||
| chr2:53745163 | T | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0112 a0001c0001t0001g0123 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+5620A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745163 | |||||||
| chr2:53745331 | T | A | 4 | a0001c0001t0009g0199 a0001c0001t0009g0200 a0001c0001t0012g0203 others(1): Show |
4 | HG02056.hp2 NA19000.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+5452A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745331 | |||||||
| chr2:53745473 | G | C | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+5310C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745473 | |||||||
| chr2:53745556 | G | A | 159 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.355+5227C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745556 | |||||||
| chr2:53745769 | CA | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+5013delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745769 | |||||||
| chr2:53746155 | G | A | 1 | a0001c0002t0007g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.355+4628C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746155 | |||||||
| chr2:53746165 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+4618C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746165 | |||||||
| chr2:53746249 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.355+4534A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746249 | |||||||
| chr2:53746424 | A | G | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.355+4359T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746424 | |||||||
| chr2:53746457 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0003g0171 |
3 | HG02080.hp2 NA18747.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.355+4326G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746457 | |||||||
| chr2:53746485 | C | CTTT | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.355+4295_355+4297d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746485 | |||||||
| chr2:53746609 | G | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0081 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+4174C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746609 | |||||||
| chr2:53746652 | G | A | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.355+4131C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746652 | |||||||
| chr2:53746669 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355+4114C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746669 | |||||||
| chr2:53746687 | C | G | 1 | a0001c0001t0004g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.355+4096G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746687 | |||||||
| chr2:53746728 | C | G | 3 | a0001c0003t0005g0343 a0003c0005t0005g0336 a0003c0005t0005g0337 |
3 | HG01106.hp2 HG01192.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.355+4055G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746728 | |||||||
| chr2:53746758 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
88 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.355+4025T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746758 | |||||||
| chr2:53746837 | T | C | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+3946A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746837 | |||||||
| chr2:53746904 | A | G | 17 | a0001c0003t0002g0277 a0001c0003t0002g0278 a0001c0003t0002g0279 others(14): Show |
17 | HG00558.hp2 HG00621.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.355+3879T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746904 | |||||||
| chr2:53747071 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.355+3712A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747071 | |||||||
| chr2:53747086 | T | G | 142 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.355+3697A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747086 | |||||||
| chr2:53747212 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+3571T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747212 | |||||||
| chr2:53747420 | C | A | 1 | a0001c0002t0002g0248 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.355+3363G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747420 | |||||||
| chr2:53747557 | G | A | 13 | a0001c0001t0003g0340 a0001c0003t0005g0311 a0001c0003t0005g0328 others(10): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+3226C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747557 | |||||||
| chr2:53747958 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0341 |
2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.355+2825A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747958 | |||||||
| chr2:53747999 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+2784T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747999 | |||||||
| chr2:53748010 | C | A | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355+2773G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748010 | |||||||
| chr2:53748093 | CAT | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+2688_355+2689d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748093 | |||||||
| chr2:53748299 | T | C | 46 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(43): Show |
46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.355+2484A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748299 | |||||||
| chr2:53748404 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.355+2379G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748404 | |||||||
| chr2:53748428 | T | A | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+2355A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748428 | |||||||
| chr2:53748510 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.355+2273C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748510 | |||||||
| chr2:53748689 | G | C | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.355+2094C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748689 | |||||||
| chr2:53748744 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.355+2039A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748744 | |||||||
| chr2:53748805 | C | T | 1 | a0001c0002t0002g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.355+1978G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748805 | |||||||
| chr2:53748806 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.355+1977G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748806 | |||||||
| chr2:53748919 | C | A | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.355+1864G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748919 | |||||||
| chr2:53749176 | G | C | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+1607C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749176 | |||||||
| chr2:53749253 | A | C | 13 | a0001c0001t0003g0340 a0001c0003t0005g0311 a0001c0003t0005g0328 others(10): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+1530T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749253 | |||||||
| chr2:53749554 | C | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+1229G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749554 | |||||||
| chr2:53749590 | T | C | 58 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+1193A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749590 | |||||||
| chr2:53749846 | A | G | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+937T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749846 | |||||||
| chr2:53750737 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355+46A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53750737 | |||||||
| chr2:53750968 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197-27A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53750968 | |||||||
| chr2:53751321 | A | T | 1 | a0001c0001t0008g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-380T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751321 | |||||||
| chr2:53751342 | C | T | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-401G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751342 | |||||||
| chr2:53751569 | T | A | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-628A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751569 | |||||||
| chr2:53751596 | C | A | 1 | a0001c0002t0002g0249 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.197-655G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751596 | |||||||
| chr2:53751632 | G | C | 5 | a0001c0001t0001g0273 a0001c0001t0004g0272 a0001c0001t0004g0274 others(2): Show |
5 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-691C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751632 | |||||||
| chr2:53751676 | A | G | 25 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(22): Show |
25 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.197-735T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751676 | |||||||
| chr2:53751979 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0032 others(2): Show |
5 | HG01255.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-1038C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751979 | |||||||
| chr2:53751991 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1050C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751991 | |||||||
| chr2:53752592 | G | A | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1651C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752592 | |||||||
| chr2:53752635 | C | G | 2 | a0001c0003t0002g0296 a0001c0003t0002g0297 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.197-1694G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752635 | |||||||
| chr2:53752716 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-1775T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752716 | |||||||
| chr2:53752727 | G | A | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1786C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752727 | |||||||
| chr2:53752747 | T | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-1806A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752747 | |||||||
| chr2:53753038 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-2097G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753038 | |||||||
| chr2:53753044 | T | TA | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-2104_197-2103i others(3): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753044 | |||||||
| chr2:53753045 | T | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(15): Show |
18 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.197-2104A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753045 | |||||||
| chr2:53753152 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-2211G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753152 | |||||||
| chr2:53753248 | A | G | 1 | a0001c0002t0002g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.197-2307T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753248 | |||||||
| chr2:53753451 | G | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-2510C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753451 | |||||||
| chr2:53753648 | T | G | 2 | a0001c0001t0001g0206 a0001c0001t0003g0205 |
2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.197-2707A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753648 | |||||||
| chr2:53753652 | G | GT | 84 | a0001c0001t0001g0064 a0001c0001t0001g0084 a0001c0001t0001g0111 others(81): Show |
86 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.197-2712dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753652 | |||||||
| chr2:53753652 | G | GTT | 15 | a0001c0001t0003g0341 a0001c0003t0001g0304 a0001c0003t0001g0305 others(12): Show |
15 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-2713_197-2712d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753652 | |||||||
| chr2:53753668 | A | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0132 others(20): Show |
24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-2727T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753668 | |||||||
| chr2:53753698 | G | A | 5 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0032 others(2): Show |
5 | HG01255.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-2757C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753698 | |||||||
| chr2:53753740 | G | A | 4 | a0001c0002t0002g0229 a0001c0002t0002g0250 a0001c0002t0002g0251 others(1): Show |
4 | NA18941.hp2 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-2799C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753740 | |||||||
| chr2:53753761 | C | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-2820G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753761 | |||||||
| chr2:53753810 | A | AT | 40 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0079 others(37): Show |
41 | HG00099.hp1 HG00621.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.197-2870dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753810 | |||||||
| chr2:53753921 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.197-2980C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753921 | |||||||
| chr2:53753982 | C | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-3041G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753982 | |||||||
| chr2:53754005 | A | T | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-3064T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754005 | |||||||
| chr2:53754108 | CA | C | 4 | a0001c0001t0003g0177 a0001c0001t0003g0195 a0001c0001t0003g0196 others(1): Show |
4 | NA18955.hp1 NA18986.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-3168delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754108 | |||||||
| chr2:53754328 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-3387C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754328 | |||||||
| chr2:53754405 | G | A | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-3464C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754405 | |||||||
| chr2:53754518 | T | G | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-3577A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754518 | |||||||
| chr2:53754594 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.197-3653C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754594 | |||||||
| chr2:53754632 | T | C | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-3691A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754632 | |||||||
| chr2:53754701 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.197-3760G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754701 | |||||||
| chr2:53754979 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0215 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197-4038A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754979 | |||||||
| chr2:53755201 | T | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-4260A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755201 | |||||||
| chr2:53755246 | G | A | 1 | a0001c0001t0004g0025 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.197-4305C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755246 | |||||||
| chr2:53755265 | G | C | 1 | a0001c0002t0002g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.197-4324C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755265 | |||||||
| chr2:53755603 | T | A | 46 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(43): Show |
46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.197-4662A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755603 | |||||||
| chr2:53755616 | G | A | 1 | a0001c0001t0004g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-4675C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755616 | |||||||
| chr2:53755643 | A | G | 47 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(44): Show |
47 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.197-4702T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755643 | |||||||
| chr2:53755715 | A | G | 2 | a0003c0005t0005g0336 a0003c0005t0005g0337 |
2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.197-4774T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755715 | |||||||
| chr2:53755791 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.197-4850G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755791 | |||||||
| chr2:53755821 | G | A | 61 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.197-4880C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755821 | |||||||
| chr2:53755917 | C | G | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4976G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755917 | |||||||
| chr2:53755970 | T | C | 52 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(49): Show |
54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.197-5029A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755970 | |||||||
| chr2:53755970 | T | G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0075 others(2): Show |
5 | NA18963.hp2 NA18964.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-5029A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755970 | |||||||
| chr2:53755977 | AC | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
26 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.197-5037delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755977 | |||||||
| chr2:53755980 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0004g0013 a0001c0001t0015g0012 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197-5039G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755980 | |||||||
| chr2:53755986 | C | A | 1 | a0001c0003t0002g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5045G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755986 | |||||||
| chr2:53755987 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-5046G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755987 | |||||||
| chr2:53756098 | GGAGGCTG others(4): Show |
G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0335 |
2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.197-5168_197-5158d others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756098 | |||||||
| chr2:53756176 | T | A | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.197-5235A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756176 | |||||||
| chr2:53756310 | T | C | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0214 others(1): Show |
4 | HG02451.hp1 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-5369A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756310 | |||||||
| chr2:53756362 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197-5421A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756362 | |||||||
| chr2:53756396 | G | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0132 others(20): Show |
24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5455C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756396 | |||||||
| chr2:53756397 | C | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0132 others(20): Show |
24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5456G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756397 | |||||||
| chr2:53756398 | A | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0132 others(20): Show |
24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5457T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756398 | |||||||
| chr2:53756547 | T | C | 229 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
232 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.197-5606A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756547 | |||||||
| chr2:53756601 | C | G | 1 | a0001c0001t0008g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.197-5660G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756601 | |||||||
| chr2:53756709 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-5768T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756709 | |||||||
| chr2:53756722 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.197-5781G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756722 | |||||||
| chr2:53756787 | A | T | 12 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-5846T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756787 | |||||||
| chr2:53756882 | T | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-5941A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756882 | |||||||
| chr2:53756932 | A | C | 39 | a0001c0001t0001g0152 a0001c0001t0003g0341 a0001c0003t0001g0304 others(36): Show |
39 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.197-5991T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756932 | |||||||
| chr2:53757117 | A | G | 53 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(50): Show |
55 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-6176T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757117 | |||||||
| chr2:53757128 | G | A | 2 | a0001c0003t0002g0020 a0001c0003t0007g0021 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-6187C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757128 | |||||||
| chr2:53757198 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0326 |
2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.197-6257C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757198 | |||||||
| chr2:53757213 | A | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
95 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.197-6272T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757213 | |||||||
| chr2:53757233 | G | C | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.197-6292C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757233 | |||||||
| chr2:53757289 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0003g0202 |
2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.197-6348C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757289 | |||||||
| chr2:53757291 | C | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0072 others(4): Show |
7 | NA18959.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-6350G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757291 | |||||||
| chr2:53757316 | G | A | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6375C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757316 | |||||||
| chr2:53757361 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.197-6420G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757361 | |||||||
| chr2:53757362 | G | A | 2 | a0001c0002t0002g0224 a0001c0002t0002g0225 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.197-6421C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757362 | |||||||
| chr2:53757366 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0078 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.197-6425C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757366 | |||||||
| chr2:53757390 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-6449C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757390 | |||||||
| chr2:53757579 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.197-6638A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757579 | |||||||
| chr2:53757686 | A | G | 189 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
192 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.197-6745T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757686 | |||||||
| chr2:53757820 | T | C | 223 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(220): Show |
226 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.197-6879A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757820 | |||||||
| chr2:53757846 | T | C | 59 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(56): Show |
59 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.197-6905A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757846 | |||||||
| chr2:53757886 | A | C | 1 | a0001c0002t0002g0262 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.197-6945T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757886 | |||||||
| chr2:53758033 | G | A | 1 | a0001c0002t0007g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.197-7092C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758033 | |||||||
| chr2:53758193 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+7184C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758193 | |||||||
| chr2:53758275 | A | C | 1 | a0006c0010t0001g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196+7102T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758275 | |||||||
| chr2:53758329 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0035 others(53): Show |
57 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+7048G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758329 | |||||||
| chr2:53758362 | G | A | 1 | a0001c0002t0006g0270 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196+7015C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758362 | |||||||
| chr2:53758615 | G | A | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+6762C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758615 | |||||||
| chr2:53758705 | A | T | 53 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0255 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+6672T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758705 | |||||||
| chr2:53758729 | G | A | 53 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0255 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+6648C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758729 | |||||||
| chr2:53758755 | C | T | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196+6622G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758755 | |||||||
| chr2:53758844 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+6533T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758844 | |||||||
| chr2:53759232 | G | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+6145C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759232 | |||||||
| chr2:53759379 | A | G | 1 | a0001c0001t0008g0194 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.196+5998T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759379 | |||||||
| chr2:53759456 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+5921T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759456 | |||||||
| chr2:53759509 | C | T | 1 | a0001c0001t0004g0131 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.196+5868G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759509 | |||||||
| chr2:53759561 | G | T | 23 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(20): Show |
23 | HG00408.hp2 HG00733.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.196+5816C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759561 | |||||||
| chr2:53759593 | C | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
87 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.196+5784G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759593 | |||||||
| chr2:53759630 | G | C | 2 | a0001c0003t0002g0281 a0001c0003t0002g0282 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+5747C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759630 | |||||||
| chr2:53759725 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196+5652C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759725 | |||||||
| chr2:53759747 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.196+5630G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759747 | |||||||
| chr2:53759748 | G | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+5629C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759748 | |||||||
| chr2:53759795 | A | T | 2 | a0001c0003t0002g0281 a0001c0003t0002g0282 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+5582T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759795 | |||||||
| chr2:53759802 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.196+5575C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759802 | |||||||
| chr2:53759813 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.196+5564C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759813 | |||||||
| chr2:53759881 | C | T | 38 | a0001c0001t0001g0152 a0001c0003t0001g0304 a0001c0003t0001g0305 others(35): Show |
38 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.196+5496G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759881 | |||||||
| chr2:53759906 | G | C | 13 | a0001c0001t0003g0340 a0001c0003t0005g0311 a0001c0003t0005g0328 others(10): Show |
13 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.196+5471C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759906 | |||||||
| chr2:53760287 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0209 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+5090C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760287 | |||||||
| chr2:53760414 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.196+4963G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760414 | |||||||
| chr2:53760422 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(143): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.196+4955T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760422 | |||||||
| chr2:53760470 | GC | G | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+4906delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760470 | |||||||
| chr2:53760644 | TA | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
87 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.196+4732delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760644 | |||||||
| chr2:53760708 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.196+4669A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760708 | |||||||
| chr2:53760752 | G | T | 1 | a0001c0003t0002g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.196+4625C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760752 | |||||||
| chr2:53760753 | A | G | 222 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.196+4624T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760753 | |||||||
| chr2:53760754 | T | C | 222 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.196+4623A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760754 | |||||||
| chr2:53760793 | G | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+4584C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760793 | |||||||
| chr2:53760885 | A | G | 221 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(218): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.196+4492T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760885 | |||||||
| chr2:53760957 | T | C | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.196+4420A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760957 | |||||||
| chr2:53761003 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196+4374G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761003 | |||||||
| chr2:53761093 | G | A | 19 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0055 others(16): Show |
19 | HG00423.hp2 HG02132.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.196+4284C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761093 | |||||||
| chr2:53761098 | G | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0004g0213 |
3 | HG03209.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.196+4279C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761098 | |||||||
| chr2:53761383 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.196+3994C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761383 | |||||||
| chr2:53761425 | G | GA | 8 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00738.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+3951dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761425 | |||||||
| chr2:53761698 | G | T | 3 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0204 |
3 | HG01515.hp1 HG01517.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.196+3679C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761698 | |||||||
| chr2:53761826 | C | G | 1 | a0001c0003t0002g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3551G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761826 | |||||||
| chr2:53761942 | G | T | 1 | a0001c0003t0002g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3435C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761942 | |||||||
| chr2:53762030 | G | T | 7 | a0001c0002t0002g0219 a0001c0002t0002g0222 a0001c0002t0002g0223 others(4): Show |
7 | HG00423.hp1 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+3347C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762030 | |||||||
| chr2:53762035 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.196+3342A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762035 | |||||||
| chr2:53762107 | G | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
115 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.196+3270C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762107 | |||||||
| chr2:53762153 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0121 |
4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3224A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762153 | |||||||
| chr2:53762171 | C | CTG | 85 | a0001c0001t0001g0049 a0001c0001t0001g0268 a0001c0001t0001g0310 others(82): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+3204_196+3205d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | |||||||
| chr2:53762171 | C | CTGTG | 4 | a0001c0001t0002g0153 a0001c0001t0003g0341 a0001c0001t0004g0323 others(1): Show |
4 | HG01243.hp2 HG03942.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3202_196+3205d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | |||||||
| chr2:53762171 | CTG | C | 49 | a0001c0001t0001g0144 a0001c0001t0001g0170 a0001c0001t0001g0172 others(46): Show |
51 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+3204_196+3205d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | |||||||
| chr2:53762171 | CTGTGTG | C | 5 | a0001c0001t0001g0273 a0001c0001t0004g0272 a0001c0001t0004g0274 others(2): Show |
5 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+3200_196+3205d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | |||||||
| chr2:53762334 | G | A | 5 | a0001c0003t0005g0311 a0001c0003t0005g0330 a0001c0003t0005g0334 others(2): Show |
5 | HG01123.hp1 HG01168.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+3043C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762334 | |||||||
| chr2:53762440 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+2937C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762440 | |||||||
| chr2:53762608 | T | C | 11 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(8): Show |
11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+2769A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762608 | |||||||
| chr2:53762847 | A | C | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+2530T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762847 | |||||||
| chr2:53763296 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+2081A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763296 | |||||||
| chr2:53763395 | C | T | 164 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
167 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.196+1982G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763395 | |||||||
| chr2:53763564 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.196+1813C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763564 | |||||||
| chr2:53763581 | A | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0209 a0001c0001t0003g0340 |
3 | HG01891.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+1796T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763581 | |||||||
| chr2:53763582 | A | G | 1 | a0001c0001t0009g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.196+1795T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763582 | |||||||
| chr2:53763781 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+1596C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763781 | |||||||
| chr2:53763785 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+1592A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763785 | |||||||
| chr2:53763840 | C | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+1537G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763840 | |||||||
| chr2:53763941 | G | C | 2 | a0001c0003t0002g0281 a0001c0003t0002g0282 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+1436C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763941 | |||||||
| chr2:53763961 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.196+1416G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763961 | |||||||
| chr2:53764085 | A | T | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+1292T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764085 | |||||||
| chr2:53764156 | T | C | 58 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+1221A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764156 | |||||||
| chr2:53764440 | A | C | 2 | a0001c0003t0007g0283 a0001c0003t0007g0284 |
2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.196+937T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764440 | |||||||
| chr2:53764542 | C | G | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+835G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764542 | |||||||
| chr2:53764570 | A | C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
196 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.196+807T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764570 | |||||||
| chr2:53764604 | A | T | 193 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
196 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.196+773T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764604 | |||||||
| chr2:53764671 | T | C | 1 | a0007c0007t0005g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.196+706A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764671 | |||||||
| chr2:53764733 | C | T | 1 | a0001c0003t0002g0309 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196+644G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764733 | |||||||
| chr2:53764758 | G | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+619C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764758 | |||||||
| chr2:53764962 | A | C | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196+415T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764962 | |||||||
| chr2:53765032 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+345C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765032 | |||||||
| chr2:53765041 | C | A | 2 | a0001c0003t0007g0283 a0001c0003t0007g0284 |
2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.196+336G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765041 | |||||||
| chr2:53765174 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0003g0205 |
2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.196+203C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765174 | |||||||
| chr2:53765645 | G | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-13-60C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765645 | |||||||
| chr2:53765722 | T | G | 47 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(44): Show |
47 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-13-137A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765722 | |||||||
| chr2:53765726 | A | G | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-141T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765726 | |||||||
| chr2:53765900 | TTCTTTGG others(22): Show |
T | 24 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(21): Show |
24 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13-344_-13-316del others(29): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765900 | |||||||
| chr2:53765936 | G | A | 2 | a0001c0003t0002g0296 a0001c0003t0002g0297 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-351C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765936 | |||||||
| chr2:53766109 | T | C | 1 | a0001c0003t0006g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-13-524A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766109 | |||||||
| chr2:53766245 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-660T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766245 | |||||||
| chr2:53766326 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0004g0120 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-13-741C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766326 | |||||||
| chr2:53766329 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-744A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766329 | |||||||
| chr2:53766350 | G | A | 137 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0148 others(134): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-13-765C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766350 | |||||||
| chr2:53766366 | G | A | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-781C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766366 | |||||||
| chr2:53766377 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0004g0052 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-13-792A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766377 | |||||||
| chr2:53766456 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0121 |
4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-871T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766456 | |||||||
| chr2:53766465 | G | C | 1 | a0001c0001t0008g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13-880C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766465 | |||||||
| chr2:53766482 | T | A | 2 | a0001c0001t0001g0132 a0001c0001t0004g0113 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-13-897A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766482 | |||||||
| chr2:53766535 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-950A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766535 | |||||||
| chr2:53766788 | C | T | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1203G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766788 | |||||||
| chr2:53766923 | T | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1338A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766923 | |||||||
| chr2:53767023 | C | A | 51 | a0001c0002t0001g0257 a0001c0002t0002g0016 a0001c0002t0002g0017 others(48): Show |
51 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-13-1438G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767023 | |||||||
| chr2:53767161 | G | A | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-1576C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767161 | |||||||
| chr2:53767356 | A | G | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-1771T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767356 | |||||||
| chr2:53767400 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-1815A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767400 | |||||||
| chr2:53767441 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13-1856G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767441 | |||||||
| chr2:53767465 | C | T | 2 | a0001c0003t0002g0301 a0001c0003t0002g0302 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13-1880G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767465 | |||||||
| chr2:53767615 | A | C | 1 | a0002c0004t0013g0011 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-2030T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767615 | |||||||
| chr2:53767683 | C | T | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-13-2098G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767683 | |||||||
| chr2:53767730 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(6): Show |
10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-2145A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767730 | |||||||
| chr2:53767746 | C | T | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-2161G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767746 | |||||||
| chr2:53767786 | C | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18612.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-13-2201G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767786 | |||||||
| chr2:53767792 | G | A | 38 | a0001c0001t0001g0152 a0001c0003t0001g0304 a0001c0003t0001g0305 others(35): Show |
38 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-13-2207C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767792 | |||||||
| chr2:53768243 | C | T | 139 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13-2658G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768243 | |||||||
| chr2:53768359 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13-2774C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768359 | |||||||
| chr2:53768543 | C | T | 204 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
207 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-13-2958G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768543 | |||||||
| chr2:53768596 | T | G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.-13-3011A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768596 | |||||||
| chr2:53768607 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-13-3022A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768607 | |||||||
| chr2:53768684 | A | G | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-3099T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768684 | |||||||
| chr2:53768753 | A | C | 12 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(9): Show |
12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-3168T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768753 | |||||||
| chr2:53768753 | A | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-13-3168T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768753 | |||||||
| chr2:53768780 | T | C | 1 | a0001c0003t0014g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3195A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768780 | |||||||
| chr2:53768818 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-13-3233T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768818 | |||||||
| chr2:53768939 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-3354T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768939 | |||||||
| chr2:53768940 | C | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
85 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.-13-3355G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768940 | |||||||
| chr2:53768947 | A | T | 1 | a0001c0003t0014g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3362T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768947 | |||||||
| chr2:53769103 | G | A | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-3518C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769103 | |||||||
| chr2:53769167 | G | C | 1 | a0001c0001t0012g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-13-3582C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769167 | |||||||
| chr2:53769351 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-3766G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769351 | |||||||
| chr2:53769418 | T | C | 24 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(21): Show |
24 | HG01358.hp1 HG01515.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13-3833A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769418 | |||||||
| chr2:53769419 | A | T | 1 | a0001c0002t0002g0226 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-13-3834T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769419 | |||||||
| chr2:53769429 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-3844T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769429 | |||||||
| chr2:53769446 | G | C | 229 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.-13-3861C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769446 | |||||||
| chr2:53769730 | C | A | 1 | a0001c0003t0006g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-13-4145G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769730 | |||||||
| chr2:53769783 | G | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4198C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769783 | |||||||
| chr2:53769799 | G | A | 3 | a0001c0003t0002g0295 a0001c0003t0002g0296 a0001c0003t0002g0297 |
3 | HG03041.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-4214C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769799 | |||||||
| chr2:53769915 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0008g0028 a0001c0001t0008g0030 others(4): Show |
7 | HG01255.hp1 HG02257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4330A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769915 | |||||||
| chr2:53769937 | C | T | 1 | a0001c0001t0009g0178 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13-4352G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769937 | |||||||
| chr2:53770021 | C | A | 45 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(42): Show |
47 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13-4436G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770021 | |||||||
| chr2:53770183 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0121 |
4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4598C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770183 | |||||||
| chr2:53770204 | C | CA | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-4620dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770204 | |||||||
| chr2:53770209 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13-4624A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770209 | |||||||
| chr2:53770328 | G | C | 2 | a0001c0002t0001g0257 a0001c0002t0002g0256 |
2 | NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-13-4743C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770328 | |||||||
| chr2:53770411 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13-4826A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770411 | |||||||
| chr2:53770487 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
23 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.-13-4902G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770487 | |||||||
| chr2:53770498 | T | TA | 7 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG01952.hp1 HG03927.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4914dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | |||||||
| chr2:53770498 | TA | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0035 others(98): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-13-4914delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | |||||||
| chr2:53770498 | TAA | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
39 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.-13-4915_-13-4914d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | |||||||
| chr2:53770498 | TAAA | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0148 others(53): Show |
56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-13-4916_-13-4914d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | |||||||
| chr2:53770498 | TAAAA | T | 58 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-13-4917_-13-4914d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | |||||||
| chr2:53770539 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-4954A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770539 | |||||||
| chr2:53770650 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0004g0052 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-13-5065T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770650 | |||||||
| chr2:53770852 | A | G | 3 | a0001c0001t0003g0145 a0001c0001t0003g0146 a0001c0001t0003g0147 |
3 | HG02630.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-13-5267T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770852 | |||||||
| chr2:53770873 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5288A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770873 | |||||||
| chr2:53771118 | C | A | 1 | a0001c0003t0004g0307 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-13-5533G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771118 | |||||||
| chr2:53771185 | A | G | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-5600T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771185 | |||||||
| chr2:53771218 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-5633G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771218 | |||||||
| chr2:53771219 | C | T | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-5634G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771219 | |||||||
| chr2:53771301 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0004g0013 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-13-5716C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771301 | |||||||
| chr2:53771317 | C | A | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-5732G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771317 | |||||||
| chr2:53771374 | G | C | 2 | a0001c0003t0005g0331 a0001c0003t0005g0332 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-13-5789C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771374 | |||||||
| chr2:53771421 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5836C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771421 | |||||||
| chr2:53771443 | T | A | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-5858A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771443 | |||||||
| chr2:53771520 | T | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-5935A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771520 | |||||||
| chr2:53771571 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13-5986T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771571 | |||||||
| chr2:53771703 | T | C | 1 | a0001c0003t0005g0343 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13-6118A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771703 | |||||||
| chr2:53771711 | G | T | 7 | a0001c0002t0002g0219 a0001c0002t0002g0222 a0001c0002t0002g0223 others(4): Show |
7 | HG00423.hp1 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-6126C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771711 | |||||||
| chr2:53771789 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-6204A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771789 | |||||||
| chr2:53771883 | T | A | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-6298A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771883 | |||||||
| chr2:53772040 | A | C | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG02080.hp1 NA18968.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-6455T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772040 | |||||||
| chr2:53772108 | A | G | 2 | a0001c0002t0002g0263 a0001c0002t0002g0264 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-13-6523T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772108 | |||||||
| chr2:53772121 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0004g0013 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-13-6536C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772121 | |||||||
| chr2:53772186 | G | GT | 83 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
86 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.-13-6602dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772186 | |||||||
| chr2:53772186 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-13-6601C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772186 | |||||||
| chr2:53772205 | A | C | 1 | a0001c0001t0001g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-13-6620T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772205 | |||||||
| chr2:53772237 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-13-6652G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772237 | |||||||
| chr2:53772335 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(6): Show |
10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-6750A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772335 | |||||||
| chr2:53772366 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-13-6781T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772366 | |||||||
| chr2:53772416 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13-6831G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772416 | |||||||
| chr2:53772425 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0003g0166 a0001c0001t0003g0341 |
3 | HG03669.hp2 NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-6840A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772425 | |||||||
| chr2:53772501 | T | G | 1 | a0001c0001t0004g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13-6916A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772501 | |||||||
| chr2:53772529 | C | T | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-6944G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772529 | |||||||
| chr2:53772637 | T | G | 58 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-13-7052A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772637 | |||||||
| chr2:53772702 | GTGTTTT | G | 55 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(52): Show |
57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-7123_-13-7118d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772702 | |||||||
| chr2:53772825 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-7240A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772825 | |||||||
| chr2:53772883 | T | C | 1 | a0001c0002t0002g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-13-7298A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772883 | |||||||
| chr2:53773085 | A | T | 1 | a0001c0001t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-13-7500T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773085 | |||||||
| chr2:53773125 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0004g0113 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-13-7540C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773125 | |||||||
| chr2:53773130 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-7545C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773130 | |||||||
| chr2:53773293 | T | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0129 |
3 | HG02015.hp2 HG03710.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-13-7708A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773293 | |||||||
| chr2:53773321 | C | CAAGATAT others(25): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7737_-13-7736i others(34): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773321 | |||||||
| chr2:53773322 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7737G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773322 | |||||||
| chr2:53773323 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7738A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773323 | |||||||
| chr2:53773324 | A | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-7739T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773324 | |||||||
| chr2:53773326 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7741C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773326 | |||||||
| chr2:53773401 | C | CT | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-7817dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773401 | |||||||
| chr2:53773418 | CTG | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-7835_-13-7834d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773418 | |||||||
| chr2:53773500 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-13-7915C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773500 | |||||||
| chr2:53773503 | T | C | 2 | a0001c0003t0005g0331 a0001c0003t0005g0332 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-13-7918A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773503 | |||||||
| chr2:53773681 | G | A | 1 | a0001c0001t0003g0340 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-8096C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773681 | |||||||
| chr2:53773719 | G | A | 2 | a0001c0003t0002g0301 a0001c0003t0002g0302 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13-8134C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773719 | |||||||
| chr2:53773801 | G | A | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-8216C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773801 | |||||||
| chr2:53773905 | C | G | 1 | a0001c0001t0004g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-13-8320G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773905 | |||||||
| chr2:53774008 | C | G | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-13-8423G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774008 | |||||||
| chr2:53774033 | C | CA | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-8449dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774033 | |||||||
| chr2:53774093 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13-8508T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774093 | |||||||
| chr2:53774499 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0004g0213 |
3 | HG03209.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-13-8914C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774499 | |||||||
| chr2:53774659 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-13-9074G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774659 | |||||||
| chr2:53774710 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-13-9125T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774710 | |||||||
| chr2:53774927 | C | A | 49 | a0001c0001t0003g0340 a0001c0003t0001g0304 a0001c0003t0001g0305 others(46): Show |
49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.-13-9342G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774927 | |||||||
| chr2:53775131 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-9546C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775131 | |||||||
| chr2:53775339 | T | TTG | 59 | a0001c0001t0001g0116 a0001c0001t0001g0268 a0001c0001t0001g0269 others(56): Show |
59 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-13-9756_-13-9755d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775339 | |||||||
| chr2:53775366 | T | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0170 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13-9781A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775366 | |||||||
| chr2:53775368 | T | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-9783A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775368 | |||||||
| chr2:53775385 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-13-9800A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775385 | |||||||
| chr2:53775404 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-13-9819C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775404 | |||||||
| chr2:53775422 | C | G | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-9837G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775422 | |||||||
| chr2:53775611 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0121 |
3 | HG01081.hp2 HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-13-10026C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775611 | |||||||
| chr2:53775723 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-10138C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775723 | |||||||
| chr2:53775876 | C | G | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0041 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13-10291G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775876 | |||||||
| chr2:53776034 | A | G | 2 | a0001c0003t0002g0320 a0001c0003t0002g0321 |
2 | HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-13-10449T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776034 | |||||||
| chr2:53776269 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-14+10552G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776269 | |||||||
| chr2:53776640 | A | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-14+10181T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776640 | |||||||
| chr2:53776751 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0003g0217 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+10070G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776751 | |||||||
| chr2:53776764 | A | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-14+10057T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776764 | |||||||
| chr2:53776823 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-14+9998T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776823 | |||||||
| chr2:53776853 | G | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+9968C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776853 | |||||||
| chr2:53777095 | C | G | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+9726G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777095 | |||||||
| chr2:53777351 | T | G | 6 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+9470A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777351 | |||||||
| chr2:53777421 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-14+9400C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777421 | |||||||
| chr2:53777589 | C | CT | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14+9231dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777589 | |||||||
| chr2:53777660 | C | T | 1 | a0001c0001t0003g0341 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-14+9161G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777660 | |||||||
| chr2:53777698 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+9123C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777698 | |||||||
| chr2:53777726 | A | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+9095T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777726 | |||||||
| chr2:53777983 | C | T | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14+8838G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777983 | |||||||
| chr2:53778010 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+8811C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778010 | |||||||
| chr2:53778149 | C | CA | 9 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0333 others(6): Show |
9 | HG01358.hp2 HG01952.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+8671dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | |||||||
| chr2:53778149 | CA | C | 85 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0035 others(82): Show |
87 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-14+8671delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | |||||||
| chr2:53778149 | CAA | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
23 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14+8670_-14+8671d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | |||||||
| chr2:53778281 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+8540T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778281 | |||||||
| chr2:53778423 | T | C | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+8398A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778423 | |||||||
| chr2:53778792 | G | T | 1 | a0001c0001t0004g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-14+8029C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778792 | |||||||
| chr2:53778810 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
79 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14+8011G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778810 | |||||||
| chr2:53778926 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+7895A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778926 | |||||||
| chr2:53778962 | C | T | 211 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
214 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-14+7859G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778962 | |||||||
| chr2:53778975 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-14+7846G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778975 | |||||||
| chr2:53778986 | A | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+7835T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778986 | |||||||
| chr2:53779002 | A | G | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-14+7819T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779002 | |||||||
| chr2:53779018 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-14+7803G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779018 | |||||||
| chr2:53779421 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-14+7400C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779421 | |||||||
| chr2:53779621 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
79 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14+7200C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779621 | |||||||
| chr2:53779886 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+6935A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779886 | |||||||
| chr2:53779999 | G | A | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+6822C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779999 | |||||||
| chr2:53780034 | A | C | 61 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(58): Show |
61 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-14+6787T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780034 | |||||||
| chr2:53780197 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14+6624T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780197 | |||||||
| chr2:53780349 | T | C | 2 | a0001c0002t0002g0263 a0001c0002t0002g0264 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-14+6472A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780349 | |||||||
| chr2:53780514 | C | T | 56 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(53): Show |
56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14+6307G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780514 | |||||||
| chr2:53780515 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0003g0205 |
2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-14+6306C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780515 | |||||||
| chr2:53780554 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-14+6267C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780554 | |||||||
| chr2:53781131 | G | A | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+5690C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781131 | |||||||
| chr2:53781271 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(6): Show |
10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+5550C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781271 | |||||||
| chr2:53781273 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-14+5548C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781273 | |||||||
| chr2:53781373 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+5448A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781373 | |||||||
| chr2:53781412 | C | CA | 7 | a0001c0001t0001g0165 a0001c0001t0002g0130 a0001c0001t0004g0131 others(4): Show |
7 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5408dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781412 | |||||||
| chr2:53781412 | CA | C | 57 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14+5408delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781412 | |||||||
| chr2:53781466 | G | T | 7 | a0001c0003t0002g0277 a0001c0003t0002g0279 a0001c0003t0002g0280 others(4): Show |
7 | HG00558.hp2 HG02083.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5355C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781466 | |||||||
| chr2:53781490 | TC | T | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+5330delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781490 | |||||||
| chr2:53781498 | T | C | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+5323A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781498 | |||||||
| chr2:53781635 | A | T | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0310 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-14+5186T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781635 | |||||||
| chr2:53781665 | T | C | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+5156A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781665 | |||||||
| chr2:53781670 | T | C | 46 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(43): Show |
48 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.-14+5151A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781670 | |||||||
| chr2:53781781 | C | T | 1 | a0001c0001t0008g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+5040G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781781 | |||||||
| chr2:53782124 | C | T | 2 | a0001c0001t0004g0026 a0004c0008t0001g0027 |
2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-14+4697G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782124 | |||||||
| chr2:53782153 | G | C | 1 | a0001c0002t0002g0265 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-14+4668C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782153 | |||||||
| chr2:53782182 | C | T | 59 | a0001c0001t0001g0310 a0001c0001t0001g0318 a0001c0001t0001g0319 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14+4639G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782182 | |||||||
| chr2:53782370 | T | C | 6 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(3): Show |
6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+4451A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782370 | |||||||
| chr2:53782425 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+4396C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782425 | |||||||
| chr2:53782543 | C | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
17 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+4278G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782543 | |||||||
| chr2:53782707 | C | T | 212 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
215 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-14+4114G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782707 | |||||||
| chr2:53783075 | G | T | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+3746C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783075 | |||||||
| chr2:53783077 | A | AT | 6 | a0001c0001t0004g0025 a0002c0004t0010g0135 a0002c0004t0010g0136 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+3743dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783077 | |||||||
| chr2:53783077 | A | T | 1 | a0001c0003t0002g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14+3744T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783077 | |||||||
| chr2:53783174 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-14+3647A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783174 | |||||||
| chr2:53783223 | C | G | 1 | a0001c0001t0001g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-14+3598G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783223 | |||||||
| chr2:53783273 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14+3548G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783273 | |||||||
| chr2:53783371 | CTGTATTT others(17): Show |
C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+3426_-14+3449d others(26): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783371 | |||||||
| chr2:53783427 | T | C | 4 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+3394A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783427 | |||||||
| chr2:53783739 | C | A | 3 | a0003c0005t0005g0336 a0003c0005t0005g0337 a0003c0005t0005g0338 |
3 | HG01106.hp2 HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-14+3082G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783739 | |||||||
| chr2:53783764 | C | T | 1 | a0002c0004t0010g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14+3057G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783764 | |||||||
| chr2:53783856 | C | A | 1 | a0001c0001t0004g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-14+2965G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783856 | |||||||
| chr2:53784138 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-14+2683A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784138 | |||||||
| chr2:53784148 | G | A | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2673C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784148 | |||||||
| chr2:53784150 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14+2671C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784150 | |||||||
| chr2:53784182 | T | C | 1 | a0001c0001t0008g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-14+2639A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784182 | |||||||
| chr2:53784242 | C | T | 126 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0267 others(123): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-14+2579G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784242 | |||||||
| chr2:53784432 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14+2389G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784432 | |||||||
| chr2:53784546 | C | G | 5 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2275G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784546 | |||||||
| chr2:53784614 | C | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0003g0145 others(4): Show |
7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2207G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784614 | |||||||
| chr2:53785323 | T | C | 1 | a0007c0007t0005g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-14+1498A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785323 | |||||||
| chr2:53785433 | T | TA | 125 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0001t0001g0150 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14+1387dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | |||||||
| chr2:53785433 | T | TAA | 6 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG01192.hp1 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1386_-14+1387d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | |||||||
| chr2:53785433 | TA | T | 65 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
68 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.-14+1387delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | |||||||
| chr2:53785529 | C | G | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+1292G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785529 | |||||||
| chr2:53785576 | C | A | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1245G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785576 | |||||||
| chr2:53785673 | C | T | 1 | a0001c0003t0002g0309 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-14+1148G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785673 | |||||||
| chr2:53785688 | CA | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+1132delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785688 | |||||||
| chr2:53785693 | A | T | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+1128T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785693 | |||||||
| chr2:53785743 | G | C | 3 | a0002c0004t0010g0136 a0002c0004t0010g0137 a0002c0004t0010g0138 |
3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14+1078C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785743 | |||||||
| chr2:53785761 | G | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1060C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785761 | |||||||
| chr2:53785773 | C | T | 34 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(31): Show |
34 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14+1048G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785773 | |||||||
| chr2:53785781 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-14+1040C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785781 | |||||||
| chr2:53785973 | T | TA | 54 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14+847dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785973 | |||||||
| chr2:53785983 | T | A | 1 | a0001c0002t0006g0270 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-14+838A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785983 | |||||||
| chr2:53786098 | G | A | 6 | a0001c0001t0001g0273 a0001c0001t0004g0271 a0001c0001t0004g0272 others(3): Show |
6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+723C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786098 | |||||||
| chr2:53786118 | C | T | 4 | a0002c0004t0010g0135 a0002c0004t0010g0136 a0002c0004t0010g0137 others(1): Show |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+703G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786118 | |||||||
| chr2:53786390 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(148): Show |
154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-14+431G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786390 | |||||||
| chr2:53786407 | T | C | 222 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-14+414A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786407 | |||||||
| chr2:53786446 | C | T | 4 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0019 others(1): Show |
4 | NA18971.hp2 NA18972.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+375G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786446 | |||||||
| chr2:53786516 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14+305A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786516 | |||||||
| chr2:53786560 | C | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0013 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+261G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786560 | |||||||
| chr2:53786701 | C | T | 1 | a0001c0001t0004g0010 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+120G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786701 | |||||||
| chr2:53786792 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14+29T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786792 |